Why IMDG compliance has become increasingly important for Vietnamese exporters

Manufacturers exporting chemicals, charcoal, batteries, industrial materials, aerosols, flammable products and other dangerous goods by sea face an increasingly complex compliance environment.

The 2024 Edition of the International Maritime Dangerous Goods Code incorporating Amendment 42-24 became mandatory on 1 January 2026.

The IMDG Code provides the regulatory framework for dangerous goods and marine pollutants transported by sea and covers key areas including: classification, packing, marking, labelling, placarding, documentation, packaging construction and testing, transport operations, segregation, stowage, and training.

For manufacturers, IMDG compliance therefore extends far beyond preparing a Safety Data Sheet before shipment. A robust system should connect:

Product Classification → Packaging → Factory Controls → Documentation → Container Packing → Carrier Acceptance.

What is the relationship between the UN Model Regulations and the IMDG Code?

The UN Recommendations on the Transport of Dangerous Goods – Model Regulations provide the internationally harmonized framework for the transport of dangerous goods.

The latest edition is Revision 24, published in 2025.

The Model Regulations address areas such as dangerous goods classification, packaging, marking, labelling, placarding and transport documentation.

The IMDG Code applies and develops relevant requirements specifically for maritime transport.

For exporters, the practical compliance sequence generally begins with:

UN Number → Proper Shipping Name → Class → Packing Group → Special Provisions → Packing Instruction → Packaging → Marks & Labels → Dangerous Goods Declaration → Container → Sea Transport.

An error at the classification stage can affect every subsequent step.

Who needs IMDG compliance consulting?

The service is particularly relevant to:

• chemical manufacturers;
• charcoal manufacturers and exporters;
• battery manufacturers;
• electronics companies shipping lithium or sodium-ion batteries;
• paint and coating manufacturers;
• solvent and adhesive manufacturers;
• aerosol manufacturers;
• industrial material exporters;
• logistics providers;
• warehouses;
• freight forwarders;
• manufacturers facing customer or carrier dangerous-goods requirements.

Service 1 – Dangerous Goods Classification Review

The first stage is a technical review of available product information, which may include: SDS, COA, Technical Data Sheet, composition, physical and chemical properties, manufacturing process, existing laboratory data, and previous transport classification.

The purpose is to establish or verify the applicable UN Number, Proper Shipping Name, Class, Subsidiary Risk, Packing Group, Special Provisions and Packing Instructions.

Where the available evidence is insufficient, additional technical information or testing may be required.

Service 2 – IMDG Compliance Gap Assessment

A factory-level assessment can cover:

• Product controls — classification and transport information.
• SDS controls — accuracy and consistency of transport information.
• Packaging — selection, approval and production control.
• Marking and labelling — package and overpack requirements.
• Container controls — inspection, packing and placarding.
• Documentation — Dangerous Goods Declaration and supporting records.
• Training — competence of personnel involved in dangerous goods activities.
• Emergency preparedness — response to damaged packages, spills, fire and other incidents.

The assessment results in a structured Gap Assessment Report and Corrective Action Plan.

Service 3 – IMDG Compliance System Development

Rather than treating every shipment as a separate emergency, manufacturers can establish a controlled compliance system. Documents may include: Dangerous Goods Register, Classification Review Procedure, Packaging Control Procedure, Marking and Labelling Checklist, Container Packing Checklist, Dangerous Goods Documentation Procedure, Training Matrix, Emergency Response Procedure, Internal Audit Checklist, and CAPA Tracker.

This allows the company to demonstrate how compliance is consistently managed.

Service 4 – UN Packaging and UN Mark Support

Dangerous goods cannot always be shipped in ordinary commercial packaging. Depending on the classification and applicable packing instruction, a package may need to meet UN specification packaging requirements.

Packaging can include: fibreboard boxes, plastic boxes, bags, drums, jerricans, composite packaging, and IBCs.

A UN Packaging support project may include: packaging design review, packaging code review, material and construction review, gross mass review, closure system review, Packaging Technical File preparation, test plan preparation, sample preparation, coordination with a competent third-party testing/approval organization, review of testing and approval documentation, and production and marking controls.

Can a manufacturer simply print a UN Mark on its packaging?

No. A UN specification marking should correspond to an appropriately tested and approved packaging design under the applicable authorization mechanism.

A company should verify: the approved packaging design, packaging code, performance level, maximum permitted mass or other applicable limits, contents covered, manufacturing specification, and marking authorization.

Changing the board grade, plastic material, dimensions, closure system, liner or other critical design characteristics may affect the validity of the approved design. This is why packaging change control should be part of the compliance system.

Service 5 – IMDG Training and Competence Development

IMDG compliance involves multiple departments. Relevant personnel may include: EHS, Production, Warehouse, Packing, Logistics, Export, Shipping Documentation, Quality, and container-loading supervisors.

Training should be relevant to actual job functions rather than limited to general awareness. A practical training programme may cover:

Classification → UN Number → Dangerous Goods List → Packaging → Marks & Labels → DGD → Container Packing → Segregation → Emergency Response.

Training records and competence assessments should be maintained.

Service 6 – Mock Audit and Shipment Readiness

Before the first shipment, a mock audit can verify whether the documented system is actually working. The review can include: physical packaging, package marks and labels, container placards, packing records, DGD, training evidence, traceability, container condition, and emergency controls.

Open issues can then be corrected before the shipment is presented to the carrier.

Special consideration for charcoal exporters

Charcoal is one of the areas receiving significant attention under IMDG Amendment 42-24. For applicable charcoal products, UN1361 CARBON, animal or vegetable origin, Class 4.2 and Special Provision 978 need particular attention.

Factory controls may need to address: production date, cooling/weathering, packing date, material temperature, approved packaging, container packing, headspace, Dangerous Goods Declaration, and carrier-specific requirements.

This means charcoal compliance begins at the manufacturing site — not at the port.

Carrier requirements can exceed baseline IMDG controls

Exporters should also understand the distinction between IMDG compliance and carrier acceptance requirements.

A carrier may introduce additional operational controls based on its risk-management policies. For example, updated 2026 requirements published for charcoal UN1361 shipments from Vietnam by a major ocean carrier include additional thermal protection and carrier-nominated vanning survey requirements.

Therefore, a good compliance programme should include a carrier-specific requirement review before shipment.

Is there an “IMDG Certificate” for a factory?

The IMDG Code should not be presented as a conventional management-system certification programme comparable to ISO 9001 or ISO 14001.

Depending on the project, a company may obtain or maintain: training completion certificates, compliance assessment reports, verification reports, third-party packaging test reports, and packaging approvals or certifications under an applicable scheme.

Where formal testing, approval or authorization must be issued by a competent third party, ISC Global and Staunchly Vietnam coordinate the process rather than replacing the legal role of that organization.

Our proposed project approach

A typical project can be structured into the following phases:

• Phase 1 – Regulatory and Classification Review
• Phase 2 – Factory IMDG Gap Assessment
• Phase 3 – Compliance System Development
• Phase 4 – UN Packaging Technical Review
• Phase 5 – Training and Competence Assessment
• Phase 6 – Third-Party Testing/Approval Coordination
• Phase 7 – Mock Container/Vanning Assessment
• Phase 8 – Final Compliance Verification

This integrated approach connects regulatory requirements with actual factory operations.

Why work with ISC Global and Staunchly Vietnam?

ISC Global focuses on training, consulting, international standards, ESG and compliance implementation. For dangerous-goods projects, the scope can include: regulatory review, IMDG gap assessment, system development, technical documentation, packaging preparation, CAPA, training, and audit readiness.

STC VN Co., Ltd. – Staunchly Vietnam supports: training, project coordination, assessment and verification, international-standard related services, and coordination with specialized testing, certification and verification partners.

Where a competent laboratory, approval organization, surveyor or other authorized third party is required, the project can be coordinated with the appropriate provider.

Contact us for IMDG and UN Packaging consulting in Vietnam

ISC Global

Hotline/Zalo: +84 933 096 426 – +84 868 591 260

Email: info@iscglobal.asia | van.pham@iscglobal.asia

Website: iscglobal.asia | iscglobal.edu.vn

As global buyers and retailers tighten sourcing requirements around traceability and deforestation-free supply chains, RSPO (Roundtable on Sustainable Palm Oil) certification has moved from a nice-to-have to a near-mandatory credential for manufacturers that purchase, process, or incorporate palm oil and its derivatives into finished products. ISC Global offers comprehensive RSPO Supply Chain Certification (RSPO SCCS) consulting, guiding manufacturers in Vietnam and across Asia through every stage — from initial gap assessment to certificate issuance and long-term system maintenance.

What Is RSPO Certification?

RSPO is an international not-for-profit organisation that brings together stakeholders across the palm oil value chain — growers, mills, processors, traders, retailers, and civil society — to develop and implement credible global standards for sustainable palm oil. Companies that do not grow or mill palm oil themselves, but purchase, use, or process palm oil and its derivatives as an ingredient — such as food manufacturers, cosmetics producers, and oleochemical companies — need to comply with the RSPO Supply Chain Certification Standard (RSPO SCCS), which verifies that a company’s system for receiving, controlling, storing, using, and tracing palm oil-derived material meets internationally recognised requirements.

This is distinct from the RSPO Principles & Criteria (P&C) — most recently updated to the 2024 version, adopted at RSPO’s 21st General Assembly — which applies primarily to growers and mills further upstream in the supply chain.

The Four RSPO Supply Chain Models

Before building a certification roadmap, every manufacturer needs to select the supply chain model that fits its operations and budget:

• Identity Preserved (IP): Certified palm oil from a single identifiable source, kept physically separate throughout the supply chain.
• Segregated (SG): Certified palm oil from multiple certified sources, still kept physically separate from conventional palm oil.
• Mass Balance (MB): Certified and non-certified palm oil may be mixed during production, provided the total volume of certified output claimed never exceeds the volume of certified input purchased. This is typically the most practical starting point for food and consumer-goods manufacturers, balancing cost with credibility.
• RSPO Credits (Book & Claim): Companies purchase RSPO credits corresponding to their palm oil usage without requiring physical segregation of the material itself.

Choosing the right model up front — usually Mass Balance for manufacturers beginning their sustainability journey — helps control implementation cost while still meeting full RSPO SCCS requirements.

Our 4-Stage Consulting Approach

ISC Global structures every RSPO SCCS project around four clear stages:

1. Kick-off, Gap Assessment & Awareness Training

We begin with a formal kick-off meeting to align on project objectives, scope, and coordination mechanisms, followed by the client forming a dedicated RSPO team (management representative, coordinator, and department representatives from purchasing, production, quality, warehouse, accounting, and sales — a requirement under the standard). We then conduct an on-site gap analysis of the existing material control and traceability system against RSPO SCCS requirements, and deliver initial RSPO awareness training for relevant staff.

2. Documentation System Development

We help build and standardise the full documentation package: procedures for receiving, controlling, and tracing palm oil-derived material; supply chain model-specific policies (particularly Mass Balance volume declaration procedures); purchasing forms, control records, and traceability documentation. At this stage we also verify that the client’s palm oil suppliers hold a valid RSPO Supply Chain licence, a prerequisite for making any RSPO claim on finished products.

3. Implementation & Evidence Building

Once the documented system is issued, we guide hands-on implementation on the factory floor — warehouse, production, and quality control areas — supporting internal audits and corrective actions to ensure the system works in practice, not just on paper.

4. Certification Audit Support

We help prepare the complete evidence package and coordinate with an RSPO-accredited independent certification body throughout the formal audit, supporting the resolution of any non-conformities identified, through to certificate issuance.

A typical project — from initial assessment to certification — takes 3 to 6 months, depending on the maturity of the client’s existing documentation and the speed of internal coordination. The RSPO Supply Chain certificate is valid for 5 years, subject to annual surveillance audits to maintain validity — certification is a continuous commitment, not a one-time event.

Why RSPO Certification Matters for Exporters

• Market access: Many global FMCG brands and retailers now require 100% RSPO-certified palm oil across their supply chains — certification is often a prerequisite simply to be considered as a supplier.
• Regulatory alignment: Traceability and deforestation-related regulations such as the EU Deforestation Regulation (EUDR) continue to push importers toward supply chains that can demonstrate verifiable, third-party-audited traceability.
• Brand credibility: Certification provides tangible, internationally recognised evidence of a company’s sustainability commitments to consumers, investors, and trading partners.
• Operational discipline: The process of building an RSPO-compliant system typically improves internal material control, reduces waste, and strengthens traceability well beyond what certification alone requires.

Why Work With ISC Global?

ISC Global brings hands-on experience across a wide range of international management system and product certifications — including ISO 9001, ISO 14001, ISO 45001, GRS, OCS, EcoVadis, SEDEX SMETA, and ISCC EU/PLUS — giving our consulting team a practical understanding of both the technical requirements of RSPO SCCS and the operational realities of manufacturing environments. In Vietnam, we work alongside our representative partner Duc Luong Services and independent audit coordination partner STC VN Co., Ltd. (Staunchly Vietnam), forming an end-to-end support ecosystem — from system consulting to certification-body coordination — that helps manufacturers move through the RSPO journey efficiently and cost-effectively.

Get in Touch for a Free Consultation

If your company is evaluating or ready to begin its RSPO Supply Chain Certification journey, our consulting team is ready to help design the right roadmap for your operations.

ISC Global

Hotline: +84 933 096 426 – +84 868 591 260

Email: info@iscglobal.asia | van.pham@iscglobal.asia

Website: iscglobal.asia | iscglobal.edu.vn

Entering Australia is not a matter of obtaining a single “TGA certificate.” The Therapeutic Goods Administration is the Australian Government regulator, while the usual commercial objective is inclusion of a kind of medical device in the Australian Register of Therapeutic Goods (ARTG) through an eligible Australian Sponsor.

Vietnamese manufacturers may already hold ISO 13485 certification, FDA establishment registration, device listings, 510(k) clearances or EU certificates. Those assets can be valuable, but they must be mapped to the Australian legal manufacturer, device scope, risk class and conformity assessment route. A disciplined market-access project prevents the company from paying for a Sponsor, MDSAP audit or new testing before the evidence strategy is understood.

1. What the TGA regulates

The TGA regulates therapeutic goods in Australia, including medical devices and IVDs, and oversees how they are manufactured, supplied, advertised and monitored. Unless an exemption, exclusion or special pathway applies, a medical device generally needs an ARTG entry before lawful supply in Australia.

KEY DISTINCTION  The TGA is a regulator, not an ISO-style standard. ARTG inclusion, Manufacturer Evidence acceptance and a TGA Conformity Assessment Certificate are different regulatory outcomes and should not be marketed as interchangeable.

The first regulatory questions are therefore product-specific: Is the product a medical device under Australian law? What is its classification? How should models be grouped into a kind of device? What GMDN term applies? Which evidence route is acceptable? How many ARTG entries are likely to be required?

2. Why an Australian Sponsor is required

A foreign manufacturer normally needs an Australian-based legal entity that meets the statutory definition of Sponsor. The Sponsor submits applications through TGA Business Services, holds the ARTG entry, maintains access to evidence and has ongoing regulatory duties while the device is supplied.

• The manufacturer remains responsible for device design, production, classification, conformity assessment procedures and technical evidence.
• The Sponsor interfaces with the TGA and supports Australian post-market reporting, corrective action and recall obligations.
• The consulting team translates regulatory requirements into a controlled data and documentation programme; it does not replace the Sponsor or regulator.

Sponsor due diligence should cover fee structure, TGA portal governance, post-market service levels, access to technical documentation, change notification, transfer rights and termination. A low annual fee is not enough if the contract creates lock-in or unclear safety responsibilities.

3. Risk classification drives evidence and cost

Australia applies a risk-based classification framework. Non-IVD devices range from Class I to Class III, with specific categories such as Class I sterile and Class I measuring; IVDs use a separate system. Classification is based on the Australian rules and may differ from the US or EU result.

Intended purpose, invasiveness, duration of contact, implantability, active functions, software, materials and specific rule wording all matter. A product name such as “dental instrument” or “monitor” is not a sufficient classification basis.

4. The end-to-end ARTG pathway

1. Confirm the product is a medical device and determine whether ARTG inclusion is required.
2. Lock intended purpose, legal manufacturer, manufacturing sites, models, accessories and key claims.
3. Apply Australian classification rules and document the rule, rationale, assumptions and open questions.
4. Determine the GMDN term, kind-of-device grouping and expected ARTG entry count.
5. Select the conformity assessment evidence route, including any use of comparable overseas regulator evidence.
6. Remediate technical documentation and Australian documents against the Essential Principles.
7. Appoint the Australian Sponsor; submit Manufacturer Evidence where required, followed by the ARTG application.
8. Respond to application audits or queries and establish annual charge, UDI, vigilance and change-control processes.

5. What a submission-ready technical dossier should contain

The depth varies by device, but a coherent dossier should allow the Sponsor and TGA to trace every key claim to risk controls and objective evidence. Typical components include:

• Device description, variants, accessories, principles of operation, intended users and patient population.
• Essential Principles checklist with document-level evidence references.
• Lifecycle risk management, benefit-risk analysis and production/post-production information.
• Design verification and validation, including biocompatibility, electrical safety/EMC, software, cybersecurity, usability, sterilisation, packaging and shelf-life where relevant.
• Clinical evaluation and clinical evidence appropriate to intended purpose and risk.
• Labelling, instructions for use, Australian Declaration of Conformity, PMS plan, vigilance and recall procedures.

6. How ISO 13485, FDA, EU and MDSAP evidence may be used

ISO 13485 is a strong QMS foundation, but it is not ARTG inclusion. TGA guidance identifies circumstances in which an ISO 13485 certificate alone is not acceptable Manufacturer Evidence for non-IVD devices. Certificate scope, sites, legal entity and the issuing body must be reviewed rather than relying on the certificate title.

The TGA recognises a range of assessments and approvals from comparable overseas regulators and assessment bodies, including certain evidence from EU bodies, the US FDA, Health Canada, MDSAP auditing organisations, Japan and Singapore. Recognition is evidence-specific. FDA establishment registration and device listing are not product clearance or approval; 510(k), De Novo or PMA evidence must be distinguished and may need supporting QMS evidence.

EVIDENCE STRATEGY  Build an Evidence Acceptance Matrix before purchasing MDSAP, new testing or direct TGA conformity assessment. The matrix should map each device and site to QMS evidence, product authorisation, technical reports, clinical support, validity dates and identified gaps.

7. What changed in 2026

TGA fees from 1 July 2026

For non-IVD medical devices, the official 2026 schedule lists an ARTG application fee of AUD 651 for Class I categories, AUD 1,244 for Class IIa/IIb and AUD 1,603 for Class III. Annual charges are separate: AUD 121 for Class I other, AUD 879 for Class I sterile/measuring, AUD 1,305 for Class IIa/IIb and AUD 1,662 for Class III/AIMD. Application audit fees may be added.

UDI commenced with higher-risk devices

From 1 July 2026, in-scope Class IIb and Class III devices must meet Australian Unique Device Identification requirements, with lower-risk classes and IVDs following later phases. Manufacturers and Sponsors should plan identifiers, packaging levels, label control, AusUDID data and change-control rules; UDI is not merely a barcode artwork task.

8. ISC Global consulting methodology

ISC Global provides training, regulatory assessment, documentation consulting and compliance coordination for medical device manufacturers. The engagement begins with a controlled decision gate so that regulatory assumptions are validated before major third-party costs are triggered.

• Executive and cross-functional training on TGA, ARTG, Sponsor, Manufacturer Evidence, UDI and post-market duties.
• Product classification, GMDN and kind-of-device/ARTG grouping analysis.
• Gap assessment of ISO 13485, FDA/EU/MDSAP evidence and technical documentation.
• Drafting or review of the Essential Principles matrix, Australian Declaration of Conformity, labelling/IFU and PMS documentation within the agreed scope.
• Australian Sponsor and laboratory/assessment-body coordination after written approval of the third-party scope and quotation.
• Submission readiness, query tracking, audit support and regulatory handover for ongoing maintenance.

9. Deliverables that support internal ownership

Consulting should leave the manufacturer with a maintainable regulatory system, not only a set of meetings. Depending on scope, deliverables may include:

• Classification and ARTG Grouping Report with rule rationale and assumptions.
• Evidence Acceptance Matrix and prioritised gap register.
• Data Request List with owners, dates and expected evidence.
• Essential Principles Evidence Matrix and Australian document set.
• Testing and standards matrix, where relevant.
• Sponsor handover pack or submission-ready dossier under defined acceptance criteria.
• Query tracker, change log and close-out/maintenance plan.

10. Indicative timeline and budget logic

For a pilot product family with a reasonably mature dossier, classification, grouping and evidence-route assessment may target the first three to four weeks. Dossier remediation and submission readiness can require several additional weeks or months. New testing, MDSAP, clinical work, direct TGA conformity assessment and application audits can extend both timeline and budget.

The official ARTG fee is only one layer. A complete first-year budget may include consulting, Sponsor, TGA charges, testing, QMS/certification, translations, samples and post-market setup. It is better to approve these items at milestones than to treat every possible cost as mandatory on day one.

• Pilot with the product family that has the strongest technical and overseas market evidence.
• Confirm the expected ARTG entry count before obtaining a Sponsor quotation.
• Approve new testing only against a documented gap and current standard edition.
• Maintain a 10-15% contingency for queries, retesting, logistics and currency movement.
• Separate professional fees, government charges and third-party invoices in the commercial proposal.

11. Professional principles

ISC Global acts as an independent adviser connecting legal requirements with design, manufacturing, quality, clinical and market evidence. The consulting approach is based on four principles:

• Evidence-based conclusions: every classification, grouping and route states its basis and assumptions.
• Transparent cost gates: Sponsor, TGA, auditing organisation and laboratory costs require an approved scope and quotation.
• No misleading equivalence: ISO 13485 or FDA registration is never presented as TGA product approval.
• Clear role separation: the TGA, Sponsor, certification body, auditing organisation and laboratory remain independent decision-makers or service providers.

Frequently asked questions

Does the TGA issue one certificate for the whole company?

No. The usual market-authorisation outcome is ARTG inclusion for a kind of medical device, supported by appropriate conformity assessment evidence. A manufacturer may have multiple ARTG entries and evidence routes.

Can a Vietnamese manufacturer submit directly to the TGA?

A foreign manufacturer normally works through an eligible Australian-based Sponsor. The Sponsor submits and holds the ARTG entry while the manufacturer remains responsible for the device and supporting evidence.

Is ISO 13485 enough?

Not by itself in many non-IVD cases. It supports the QMS, but acceptable Manufacturer Evidence depends on device type, class and evidence route.

Does FDA registration count as Australian approval?

No. Establishment registration and device listing are not product clearance or approval. Any 510(k), De Novo or PMA evidence must be assessed for its Australian relevance and supporting QMS evidence.

How many products can be included in one ARTG entry?

The entry is based on a kind of medical device, not simply a catalogue. Models may be grouped only when they meet the applicable criteria; a grouping assessment is required.

Can a consultant guarantee an ARTG inclusion date?

No responsible consultant should guarantee the regulator’s decision or processing time. The consultancy can commit to defined deliverables and response support within its control.

Contact our business advisory team

Discuss your product classification, evidence route, dossier readiness and Australian market-access plan with our consulting team.

ISC Global

Hotline / Zalo: +84 933 096 426  |  +84 868 591 260

Email: info@iscglobal.asia  |  van.pham@iscglobal.asia

Website: iscglobal.asia  |  iscglobal.edu.vn

What Is RecyClass and Why Does It Matter to Vietnamese Manufacturers?

For plastic recyclers and manufacturers supplying European and international customers, simply describing a product as “recycled plastic” may no longer satisfy customer expectations.

Buyers increasingly expect evidence regarding the origin of plastic waste, pre-consumer versus post-consumer status, recycled-content claims, batch traceability, production records, input-output reconciliation and independent third-party verification.

RecyClass provides science-based methodologies, technical guidance and certification schemes designed to improve circularity and transparency across the plastics value chain.

Which RecyClass Certification Does Your Company Need?

Choosing the right scheme is the first critical decision.

Recycling Process Certification

This scheme is intended for plastic recyclers processing pre-consumer and/or post-consumer plastic waste into recycled plastic products. Typical candidates may include producers of recycled PET flakes and pellets, recycled HDPE, recycled LDPE/LLDPE, recycled PP and other eligible recycled polymer outputs.

Recycled Plastics Traceability Certification

This certification addresses traceability of recycled plastics further along the value chain and is relevant to companies using or handling recycled plastics beyond the recycling stage.

Recyclability Certification

For companies seeking to demonstrate the recyclability performance of plastic packaging, RecyClass operates separate recyclability certification schemes and methodologies.

EN 15343 and Recycled Plastic Traceability

A robust system should allow a company to demonstrate a logical evidence chain: Waste Supplier → Incoming Material → Receiving Record → Storage → Recycling Line → Production Batch → Recycled Output → Finished-Goods Warehouse → Sales Transaction.

The reverse trace should also work. Starting from a finished recycled product, the company should be able to trace relevant records back through production and ultimately to the recycled input.

Special Requirement for Recycling Sites: Module C

For Recycling Process Certification, applicants outside EU27+3 need to pay particular attention to Module C – Corporate Social Responsibility. A Vietnamese recycler should therefore include Module C in its readiness assessment from the beginning.

What About Food-Contact rPET?

Where recycled material is intended for food-contact applications, additional requirements may apply, including Module A where relevant. Companies should not market Module A as a standalone food-safety approval or as a substitute for EU food-contact regulatory compliance.

How Does the Certification Process Work?

A typical journey includes: Eligibility Review → Scope Definition → Certification Body Selection → Application & NDA → Document Preparation → On-site Audit → Corrective Actions, if applicable → Certification Decision → Renewal.

How Much Does RecyClass Certification Cost?

There is no single audit price applicable to every factory. An accurate quotation should normally consider the number of sites, polymers, product families, recycled-content variations, production lines, product codes/references, output variability, applicable modules and auditor travel requirements.

What Should Be Prepared Before the Audit?

ISC Global recommends building readiness around five pillars: certification scope; traceability; material flow and records; procedures and responsibilities; and internal verification.

How ISC Global Supports Your RecyClass Journey

Our consulting approach may include Initial Gap Assessment, Certification Scope Mapping, EN 15343 & RecyClass Training, Documentation Development, Traceability & Material-Flow Exercises, Module C / Module A Readiness, Internal Audit & Pre-assessment and Certification Support.

ISC Global acts as a training and consulting partner. The final certification decision remains with the competent third-party Certification Body.

Start With a RecyClass Readiness Assessment

If your factory produces or uses recycled plastics and is receiving RecyClass, EN 15343 or recycled-content requirements from European customers, the most efficient first step is to determine the correct certification route and assess your existing evidence.

Contact for Business Consulting

ISC Global
Hotline / Zalo: +84 933 096 426 – +84 868 591 260
Email: info@iscglobal.asia | van.pham@iscglobal.asia
Website: iscglobal.asia | iscglobal.edu.vn

A credible GRS programme connects certified inputs, transaction documents, physical or documentary traceability, volume reconciliation, responsible production controls and accurate claims. ISC Global helps manufacturers implement this system through online consulting plus on-site verification, while trading companies can receive a streamlined online programme focused on contracts, invoices, Scope Certificates and Transaction Certificates.

What is the Global Recycled Standard?

The Global Recycled Standard (GRS) is an international, voluntary, full-product standard owned by Textile Exchange. It establishes requirements for third-party certification of recycled content and chain of custody and includes social, environmental and chemical requirements for relevant processing operations. It is used by recyclers, processors, manufacturers, traders and other supply-chain organisations seeking independently verified recycled-material claims.

GRS 5.0 became effective on 1 July 2026 and may be used immediately. It becomes mandatory for audits conducted from 31 December 2026. The update is targeted rather than a full redesign: it strengthens reclaimed-material data tracking, introduces the revised Reclaimed Material Declaration Form (RMDF), and clarifies the role of the first certified entity in the recycling supply chain.

The 20% and 50% recycled-content thresholds

GRS can be used as a business-to-business tool for products containing at least 20% recycled material. Product-specific, consumer-facing GRS labelling requires at least 50% recycled content and compliance with the applicable claims and logo policy. Neither threshold provides automatic permission to use the logo: the certified scope, transaction evidence and approval requirements still apply.

GRS does not certify product quality or replace legal compliance, product safety testing, customer Restricted Substance Lists or market-specific environmental-claim laws. Claims must be written narrowly and supported by the exact certified attribute.

Who needs GRS certification consulting?

• Manufacturers of yarn, fabric, apparel, accessories, plastics, packaging and other intermediate or finished products containing recycled material.
• Processors involved in dyeing, printing, coating, laminating, finishing, assembly or subcontracted production within a GRS product flow.
• Trading, import-export or offshore entities that buy, own, invoice or sell GRS products, even when goods ship directly from the factory to the customer.
• Existing certificate holders adding products, processes, sites, warehouses or subcontractors, or preparing for recertification.
• Recyclers and primary processors preparing for GRS 5.0, the revised RMDF and the Materials Matter transition.

Our consulting methodology

1. Scope and transaction mapping

We review legal entities, sites, products, recycled materials, processes, warehouses, subcontractors and commercial flows. The resulting scope map and transaction map identify who buys, sells, pays, owns, processes and ships the product, and whose name appears on contracts, invoices, transport documents, Scope Certificates and Transaction Certificates.

2. Clause-based gap assessment

Each gap is linked to the applicable requirement, risk, owner, required document, operating evidence and target date. The assessment is built around the client’s actual material and data flow rather than a generic checklist.

3. Practical management-system documentation

• GRS system plan, scope register and responsibility matrix.
• Supplier approval and validation of incoming Scope Certificates and Transaction Certificates.
• Receiving, identification, segregation, lot traceability, production, subcontracting and shipment controls.
• Bills of material, recycled-content calculations, process-loss logic and volume reconciliation.
• Social, health and safety, environmental and chemical-management procedures appropriate to the scope.
• Claims, logo, sales-document and outgoing Transaction Certificate controls.

4. Role-based training

Management, the GRS team, purchasing, warehouse, production, quality, EHS/HR, sales, logistics and trading personnel receive role-specific training. Sessions use real or simulated documents so participants can explain their controls and retrieve evidence during an audit interview.

5. System implementation and evidence review

We review completed forms and operating records, run backward and forward traceability tests, test volume reconciliation, and verify that written procedures match actual practices. Issues are converted into corrective actions with clear owners and evidence requirements.

6. Mock audit and certification support

The readiness review covers documents, interviews and the site where applicable. We support application review, audit preparation and corrective-action responses. Certification findings and decisions remain entirely independent and are controlled by the selected approved Certification Body.

Consulting model for manufacturing sites: online plus on-site

Online workshops are efficient for document development, data review and action tracking. On-site work is essential when consultants need to observe receiving, warehouse identification, production flow, rework, waste, chemical storage, worker safety, environmental controls and staff interviews. A medium-sized factory programme may use an initial site review and a later mock audit, with remote support in between.

• Walk-through from receiving to shipment, including off-site storage and subcontracting interfaces.
• Sampling of lots, labels, production orders, material issues, output records and inventory status.
• Review of social, occupational health and safety, environmental and chemical controls at the point of use.
• Live traceability and mass-balance exercises with process owners.
• Interview coaching focused on understanding, not scripted answers.

Consulting model for trading companies: streamlined online delivery

A trading company with electronic records and no physical handling can usually complete consulting and training online. The system focuses on legal identity, ownership, documentary chain of custody, certified quantities and claims. The Certification Body determines whether and how the certification audit is conducted.

• Order-to-invoice and direct-shipment mapping.
• Supplier/customer approval and Scope Certificate monitoring.
• Incoming and outgoing Transaction Certificate register, quantity allocation and status tracking.
• Claims and logo approval workflow for websites, quotations and sales documents.
• One sample transaction exercise and one complete traceability test.
• Remote mock interview and nonconformity-response support.

Key technical controls we test

Scope Certificates and Transaction Certificates

A Scope Certificate confirms that an organisation is qualified for the listed products and processes; it does not prove that every shipment is certified. A Transaction Certificate supports the certified status of specific products and transaction details. Textile Exchange states that certified products must be accompanied by the required TC evidence.

Volume reconciliation

Certified inputs, outputs, opening and closing inventory, process losses, rejects, rework and sales must reconcile within a defined period. Where recycled and virgin materials have different loss rates, the mass-balance method must account for the difference. Traders also need quantity allocation controls so the same certified volume is not sold twice.

Social, environmental and chemical management

Manufacturing sites need assigned responsibilities, policies, legal-compliance tracking, records and training. Chemical controls include an accurate inventory, supplier information, Safety Data Sheets and evidence that chemical inputs used for GRS production meet the applicable acceptance criteria. GRS chemical controls do not replace final-product RSL compliance or legal testing obligations.

Reclaimed-material data under GRS 5.0

The first certified entity in the recycling supply chain has enhanced responsibilities for supplier authorisation records, supplier agreements, revised RMDF collection, incoming-material inspection and outgoing TCs. Even downstream organisations should understand the change because it affects the reliability and continuity of upstream evidence.

Typical deliverables

• Confirmed scope and transaction map.
• Customised management-system manual, procedures, forms and registers.
• Training materials and attendance/competence evidence.
• Supplier, Scope Certificate and Transaction Certificate verification tools.
• Traceability-test and volume-reconciliation workbooks.
• Gap register, mock-audit report, corrective-action tracker and certification-audit support.

Timing and commercial structure

A 14-18 week implementation window may be suitable for a medium-sized, responsive project with available certified inputs and committed process owners. It is a planning estimate for consulting readiness, not a guaranteed certification date. Certification Body scheduling, audit duration, nonconformity closure and certificate issuance follow a separate independent process.

Consulting and training fees are scoped by legal entities, sites, products, processes, headcount, subcontractors, languages, on-site days and evidence maturity. Third-party audit and certification fees are quoted and paid separately under the relevant arrangement with the certification service provider or Certification Body.

Frequently asked questions

Can a two-person trading company obtain GRS certification?

Yes, company size is not the determining factor. Responsibilities, document control, transaction evidence and staff competence must be clear. The applicable scope and any exemption should be confirmed with the Certification Body.

Can all consulting be delivered online?

Trading-company consulting can often be delivered online. Manufacturing projects normally benefit from on-site reviews. The audit method is independently determined by the Certification Body.

Does a valid supplier Scope Certificate make our shipment certified?

No. The product must be within the supplier’s scope and the transaction must be supported by the required Transaction Certificate and consistent commercial documents.

Does GRS certification allow us to use the logo on every product?

No. Product-specific labelling requires at least 50% recycled content, an eligible certified supply chain and compliance with the applicable claims/logo approval rules.

Does consulting guarantee certification?

No. Consulting improves readiness and supports corrective action. Audit conclusions and certification decisions remain with the independent approved Certification Body.

Contact our enterprise advisory team

Discuss your certification scope, recycled-material flow and a suitable online/on-site implementation model with our team.

ISC Global

Hotline/Zalo: +84 933 096 426 – +84 868 591 260  |  Email: info@iscglobal.asia; van.pham@iscglobal.asia  |  Website: iscglobal.asia; iscglobal.edu.vn

The European Union (EU) has just established a historic milestone for global trade with the Packaging and Packaging Waste Regulation (PPWR). This is not merely an environmental policy; it is a mandatory “technical barrier” that will reshape the entire supply chain of goods entering the European market.

So, what exactly is PPWR, which industries are in its crosshairs, and how should exporting businesses prepare to stay in the game?

1. WHAT IS PPWR? THE HISTORIC SHIFT

PPWR (officially Regulation (EU) 2025/40) is a comprehensive legislative framework designed to manage the entire lifecycle of packaging—from design and raw materials to collection and recycling.

The Core Difference: Previously, Directive 94/62/EC (PPWD) served as a “guiding framework,” allowing the 27 EU member states flexibility in its application. However, PPWR is a Regulation, meaning it is directly, uniformly, and immediately enforceable across the entire European Union. Starting in August 2026, all exporters, regardless of size or country of origin, must comply with a single, stringent set of technical standards to enter the EU.

2. THE MOST IMPACTED INDUSTRIES

While PPWR applies to all types of packaging circulating in Europe, the level of impact varies depending on the specific characteristics of each export sector:

• Food & Beverage (F&B): This sector faces the strictest scrutiny. Food processors and agricultural exporters will immediately confront bans on “forever chemicals” (PFAS) and BPA limits in food-contact packaging. Furthermore, the ban on single-use plastic packaging for fresh produce (under 1.5kg) and small condiment sachets will force a complete overhaul of packaging specifications.
• Textiles & Footwear: The primary impact lies in transportation and secondary packaging (e.g., shoeboxes, protective wraps, e-commerce bags). Footwear and apparel factories must redesign boxes to ensure the empty space ratio does not exceed 50%. Simultaneously, transitioning to Post-Consumer Recycled (PCR) plastics will require close alignment with chain-of-custody standards like the Global Recycled Standard (GRS).
• Wood, Furniture & Industrial Goods: Manufacturers of wooden furniture and industrial equipment often use large volumes of shrink wrap, adhesive tape, and oversized cartons. This group must pay special attention to the strict concentration limits for four heavy metals (Lead, Cadmium, Mercury, Chromium VI) across all packaging materials and industrial protective coatings.
• E-commerce: Strictly bound by the empty space ratio requirement (must be under 50%) to end the practice of over-packaging, which wastes materials and increases transport emissions.

3. 4 “DO-OR-DIE” TECHNICAL REQUIREMENTS

To meet the new regulations, factories and manufacturers must review and adapt to these four technical thresholds:

• Absolute Ban on Hazardous Chemicals: From August 2026, food-contact packaging will be banned if it contains PFAS above the threshold (e.g., >50 ppm for Total Fluorine). The total concentration of heavy metals in any packaging type must also not exceed 100 mg/kg.
• “Design for Recycling” (DfR) Standards: By 2030, 100% of packaging must be certified as recyclable at scale. Complex multi-layer structures (like paper laminated with thin aluminum/plastic films) face the risk of being banned. Businesses will be forced to shift towards mono-material designs.
• Empty Space Ratio: A strict requirement for optimized design, eliminating unnecessary padding layers and oversized packaging.
• Mandatory Recycled Content (PCR): Newly manufactured plastic packaging must contain a mandatory percentage of post-consumer recycled plastic. By 2030, this quota ranges from 10% to 35% (depending on the packaging type), surging to 50-65% by 2040.

4. IMPLEMENTATION TIMELINE: TIME IS RUNNING OUT

This transition leaves no room for hesitation. The legal roadmap for PPWR is set:

• February 11, 2025: The Regulation officially entered into force.
• August 12, 2026: Mandatory compliance with PFAS and heavy metal limits. Businesses must provide an EU Declaration of Conformity (DoC) and accompanying technical testing documentation for their shipments.
• January 1, 2030: Mandatory enforcement of DfR standards, PCR quotas, and the ban on certain single-use plastic packaging.

Failure to comply with PPWR not only risks customs rejections at EU borders but also exposes unsustainable packaging to exorbitant Extended Producer Responsibility (EPR) fees.

5. ISC GLOBAL – YOUR PARTNER IN CONQUERING THE GREEN MARKET

The complexity of PPWR requires businesses to adopt a comprehensive transition strategy, from auditing material suppliers to scientific testing. As a leading strategic consultant in ESG and sustainability, ISC Global provides an in-depth ecosystem of services to help cross-sector businesses navigate PPWR barriers safely and cost-effectively:

• Supply Chain Gap Analysis & Auditing: We review your entire current packaging portfolio and develop Supplier Audit criteria to screen for chemical risks from your packaging vendors.
• DfR Strategy & Material Substitution: We assist businesses in finding safe alternative materials (PFAS-free) and optimizing packaging design (reducing empty space, shifting to mono-materials) to meet the 2030 targets.
• Integration of International Sustainability Certifications: We build a roadmap for implementing and achieving material certifications such as GRS, ISCC EU, or FSC, giving your products a definitive competitive edge.
• Compliance Documentation (DoC) Support: We guide the process of submitting samples to independent labs for testing, compiling technical files, and issuing the EU Declaration of Conformity.
• GHG Inventory (Scope 3) Integration: We unlock the value of packaging optimization by recording it directly as Scope 3 emission reductions. ISC Global helps transform “legal compliance costs” into a major advantage on ESG rating platforms like EcoVadis and SMETA.

Adapting to PPWR is no longer just about protecting export market share; it is a declaration of a company’s capability and responsibility on the global stage.

Ready for a green packaging supply chain? Contact ISC Global today for in-depth consulting on the PPWR compliance roadmap tailored specifically to your industry.

Contact us to download the bilingual English-Vietnamese PDF standard: from only $50

On the path toward integration and export, correctly understanding and applying international standards is essential. Yet language and technical terminology often pose real barriers. We are pleased to introduce our bilingual (English – Vietnamese) standards documentation service, translated by our own team of certification consultants.

What We Provide

• A clause-by-clause bilingual comparison, easy to consult and file.

• Professional Vietnamese translation in correct technical terminology, ready to use.

• Interpretation notes and application guidance from hands-on experts.

• Fast delivery in editable, easy-to-store PDF/Word format.

Standards Covered

ISO management systems (9001, 14001, 45001, 37001); sustainability certifications (ISCC, FSC, VFCS/PEFC); textiles and recycled materials (GRS, OCS, OEKO-TEX); social responsibility and ESG (SMETA, EcoVadis, Fairtrade), and many other industry standards upon request.

Why Choose Us

Our documents are translated by professionals who directly consult on and audit certifications, so the translation is accurate not only in language but also in real-world application — saving you time and reducing errors when preparing documentation.

Pricing

From only USD 50 per document, depending on length and complexity. Please send us the standard name to receive a free, accurate quotation.

How to Order

1. Contact us with the name of the standard you need.

2. Receive a quotation and delivery time.

3. Make payment and receive your document by email.

Payment

Bank transfer via QR code (provided with the quotation), or via PayPal: ducluongservices@gmail.com.

We look forward to accompanying you on your certification journey.

Best regards,

CONTACT INFORMATION

Hotline: +84 933096426 – +84 868 591 260

Email:

• info@iscglobal.asia
• van.pham@iscglobal.asia

Website:

• https://iscglobal.asia/
• https://iscglobal.edu.vn/

WEEE (Waste Electrical and Electronic Equipment) refers to waste arising from electrical and electronic equipment. It is one of the fastest-growing waste streams in the European Union (EU), generated from products such as mobile phones, computers, household appliances, lighting equipment, displays, medical devices, telecommunications equipment and many other electrical and electronic products.

To address this issue, the EU established WEEE Directive 2012/19/EU, which sets requirements for the prevention and management of waste electrical and electronic equipment while promoting separate collection, reuse, recycling and recovery of resources from products at the end of their life cycle.

For manufacturers, importers and businesses placing electrical and electronic equipment on the EU market, WEEE is not only an environmental requirement. It is also closely linked to Extended Producer Responsibility (EPR) and may involve obligations relating to registration, reporting, financing, collection and proper treatment of WEEE.

WHAT IS WEEE?

WEEE stands for Waste Electrical and Electronic Equipment.

Under the WEEE Directive, Electrical and Electronic Equipment (EEE) generally refers to equipment that is dependent on electric currents or electromagnetic fields to function, or equipment used for the generation, transfer or measurement of such currents and fields, within the voltage limits specified by the Directive.

When electrical or electronic equipment is discarded and becomes waste, it is considered WEEE. The definition may also cover components, sub-assemblies and consumables that are part of the equipment when it is discarded.

The WEEE Directive aims to reduce the generation of electrical and electronic waste, increase separate collection and appropriate treatment, promote reuse and recycling, and facilitate the recovery of valuable materials from discarded equipment.

WHY IS WEEE IMPORTANT IN THE EU?

Electrical and electronic equipment is becoming increasingly important in both everyday life and industrial activities. At the same time, technological development and shorter product life cycles are contributing to a rapid increase in the amount of discarded equipment.

WEEE is a particularly important waste stream because it may contain both hazardous substances and valuable materials or critical raw materials. If WEEE is not collected and treated properly, these substances may create risks to the environment and human health. However, when properly collected and recycled, WEEE can become an important source of secondary raw materials and contribute to the development of a Circular Economy.

According to the European Commission, approximately 14.4 million tonnes of EEE were placed on the EU market in 2022, while around 5 million tonnes of WEEE were collected, equivalent to approximately 11.2 kg per person.

These figures demonstrate why WEEE management has become an increasingly important part of the EU’s environmental and circular economy policies.

WHICH PRODUCTS FALL UNDER THE WEEE SCOPE?

The scope of WEEE is relatively broad and covers a wide range of electrical and electronic equipment used in households, offices, industrial facilities and specialized sectors.

Since 15 August 2018, the WEEE Directive has classified EEE into six main categories:

• Temperature exchange equipment: refrigerators, freezers, air-conditioning equipment, heat pumps and similar products.
• Screens, monitors and equipment containing screens: televisions, computer monitors, laptops and equipment with screens larger than 100 cm².
• Lamps: certain types of lamps, including relevant fluorescent and LED lighting products.
• Large equipment: equipment with an external dimension greater than 50 cm, such as washing machines, tumble dryers, dishwashers, electric cookers and other large equipment.
• Small equipment: equipment with no external dimension greater than 50 cm, including various small household and electronic appliances.
• Small IT and telecommunications equipment: mobile phones, GPS devices, routers, computers, printers, telephones and other small IT and telecommunications equipment.

However, not every electrical product automatically falls within the scope of WEEE. The Directive also specifies a number of exclusions and special cases. Therefore, businesses should assess each product and its intended use before determining the applicable WEEE obligations.

WHO IS CONSIDERED A “PRODUCER” UNDER WEEE?

One of the most important aspects for businesses exporting to the EU is that the term “Producer” under WEEE does not simply refer to the company that physically manufactures a product.

Depending on the business model and the applicable national legislation, a company may be considered a Producer if it:

• Manufactures and sells electrical or electronic equipment under its own brand;
• Resells equipment under its own brand even though it was manufactured by another company;
• Places EEE from a non-EU country or another EU Member State on the market of a Member State;
• Sells EEE directly to users in an EU Member State through distance selling, depending on the applicable requirements.

This is particularly important for Vietnamese companies selling products directly into the EU. The fact that a product is manufactured in Vietnam does not automatically mean that the company has no WEEE obligations.

Businesses need to determine who places the product on the market in each EU country, how the product is sold, and what role the company plays in the supply chain.

WEEE REGISTRATION AND EPR IN THE EU

An important part of WEEE Compliance is Producer registration and the implementation of Extended Producer Responsibility (EPR).

The WEEE framework requires EU Member States to establish registration systems for producers and systems for collecting and reporting information relating to EEE and WEEE. Producers may also have financial responsibility for the collection, transportation, treatment, recovery and environmentally sound disposal of WEEE, depending on the applicable national requirements.

However, businesses should not assume that one WEEE registration automatically covers the entire EU market.

Although the WEEE Directive establishes the EU-level legal framework, its requirements are implemented through the legislation and administrative systems of individual Member States. As a result, registration, EPR, collection and reporting requirements may differ from one country to another.

Businesses should therefore identify the EU countries where their products are placed on the market, their sales model and their legal role in the supply chain before determining the applicable WEEE and EPR obligations.

For this reason, WEEE Compliance is often addressed together with EPR Compliance, rather than being treated solely as a waste management requirement.

WEEE COLLECTION, TREATMENT AND RECYCLING

One of the core objectives of the WEEE Directive is to ensure that electrical and electronic equipment, once it becomes waste, is separately collected and properly treated.

The Directive establishes collection targets at the Member State level. Since 2019, the collection target has been at least 65% of the average weight of EEE placed on the market in the preceding three years or 85% of WEEE generated in the territory, depending on the calculation method applied under the Directive.

These are national-level targets and should not simply be interpreted as requiring each individual company to collect 65% of its own products.

Once collected, WEEE must be delivered to appropriate treatment facilities. The Directive also establishes requirements for the selective treatment of hazardous components and sets recovery and recycling targets for different WEEE categories.

The ultimate objective is not simply to reduce the amount of waste sent to landfill or disposal, but to maximize reuse, recycling and recovery of valuable materials, thereby supporting a circular economy.

THE WEEE SYMBOL – CROSSED-OUT WHEELED BIN

One of the most recognizable elements of WEEE Compliance is the crossed-out wheeled bin symbol.

The symbol informs users that the product should not be disposed of together with ordinary household waste, but should instead be separately collected for appropriate treatment or recycling.

Under the WEEE Directive, the symbol must be clearly visible, legible and indelible. Depending on the product and applicable requirements, it may need to appear directly on the equipment, packaging, instructions for use or other relevant documentation.

Therefore, when preparing products for the EU market, businesses should review both the technical product requirements and applicable WEEE marking requirements.

WHAT IS THE DIFFERENCE BETWEEN WEEE AND ROHS?

WEEE and RoHS are often mentioned together because both apply to electrical and electronic equipment. However, they address different areas of environmental compliance.

A simple way to understand the difference is:

RoHS focuses on “what is inside the product”, while WEEE focuses on “what happens to the product when it becomes waste”.

Therefore, WEEE and RoHS should not be considered interchangeable requirements. A product may need to comply with both frameworks when it falls within their respective scopes.

WHAT SHOULD VIETNAMESE BUSINESSES CONSIDER WHEN EXPORTING ELECTRICAL AND ELECTRONIC PRODUCTS TO THE EU?

For Vietnamese manufacturers and exporters, WEEE Compliance should be considered from the early stage of preparing products for the EU market rather than after products have already been sold.

First, the company should determine whether the product falls within the WEEE scope and identify its applicable WEEE category. The company should then determine whether it is considered a Producer in the destination country, how the products are sold, and how EPR responsibilities need to be fulfilled.

Key areas to review include:

• Determining whether the product falls within the WEEE scope;
• Identifying the Producer and the relevant EU country or countries;
• Checking WEEE Registration requirements;
• Determining applicable EPR obligations and implementation mechanisms;
• Reviewing WEEE marking and product information requirements;
• Establishing reliable data on product quantities and weights placed on the market for reporting purposes;
• Determining appropriate collection, treatment and recycling arrangements.

Businesses selling products online or directly to consumers in the EU should pay particular attention to EPR responsibilities, as online sales can create additional compliance considerations depending on the market and business model.

WEEE AND THE EU CIRCULAR ECONOMY

WEEE is increasingly connected to the EU’s broader Circular Economy strategy. Instead of treating end-of-life products simply as waste, the EU seeks to extend product lifetimes and increase opportunities for repair, reuse, recycling and material recovery.

The European Commission’s 2025 evaluation of the WEEE Directive identified several areas for improvement, including the scope of the legislation, WEEE collection rates, recovery of critical raw materials, harmonization of EPR systems and WEEE treatment requirements.

This demonstrates that WEEE Compliance is likely to remain an important area for manufacturers and exporters of electrical and electronic equipment seeking access to the European market.

ISC GLOBAL WEEE COMPLIANCE SERVICES

For businesses currently exporting or planning to place electrical and electronic equipment on the EU market, identifying WEEE obligations at an early stage can help reduce regulatory risks, avoid unnecessary costs and support a smoother market entry process.

ISC Global provides WEEE & EPR Compliance consulting services to support businesses in assessing and implementing requirements related to the management of waste electrical and electronic equipment in the EU market.

Depending on the product and target market, our services may include WEEE applicability assessment, product classification, Producer status assessment, country-specific regulatory review, WEEE Registration support, EPR/PRO consultation, review of WEEE marking and product information, as well as support in preparing data and compliance documentation for reporting.

By integrating WEEE Compliance with EPR and other applicable environmental requirements, businesses can establish a more comprehensive approach to product responsibility throughout the product life cycle.

Conclusion

WEEE is more than a regulation concerning the disposal of electronic waste. It is an important part of the EU’s product end-of-life management framework and is closely connected with EPR, separate collection, reuse, recycling, resource recovery and the Circular Economy.

For Vietnamese businesses manufacturing and exporting electrical and electronic equipment to the EU, WEEE Compliance should be assessed based on the specific product, destination country and business model. WEEE Registration, Producer Responsibility, EPR obligations and WEEE marking requirements are key areas that should be evaluated before placing products on the EU market. Taking a proactive approach to WEEE Compliance can help businesses meet EU environmental requirements, reduce market-access risks, improve supply chain transparency and align their products with the EU’s growing focus on sustainable production and the Circular Economy.

Contact us to download the bilingual English-Vietnamese PDF standard: from only $50

On the path toward integration and export, correctly understanding and applying international standards is essential. Yet language and technical terminology often pose real barriers. We are pleased to introduce our bilingual (English – Vietnamese) standards documentation service, translated by our own team of certification consultants.

What We Provide

• A clause-by-clause bilingual comparison, easy to consult and file.

• Professional Vietnamese translation in correct technical terminology, ready to use.

• Interpretation notes and application guidance from hands-on experts.

• Fast delivery in editable, easy-to-store PDF/Word format.

Standards Covered

ISO management systems (9001, 14001, 45001, 37001); sustainability certifications (ISCC, FSC, VFCS/PEFC); textiles and recycled materials (GRS, OCS, OEKO-TEX); social responsibility and ESG (SMETA, EcoVadis, Fairtrade), and many other industry standards upon request.

Why Choose Us

Our documents are translated by professionals who directly consult on and audit certifications, so the translation is accurate not only in language but also in real-world application — saving you time and reducing errors when preparing documentation.

Pricing

From only USD 50 per document, depending on length and complexity. Please send us the standard name to receive a free, accurate quotation.

How to Order

1. Contact us with the name of the standard you need.

2. Receive a quotation and delivery time.

3. Make payment and receive your document by email.

Payment

Bank transfer via QR code (provided with the quotation), or via PayPal: ducluongservices@gmail.com.

We look forward to accompanying you on your certification journey.

Best regards,

CONTACT INFORMATION

Hotline: +84 933096426 – +84 868 591 260

Email:

• info@iscglobal.asia
• van.pham@iscglobal.asia

Website:

• https://iscglobal.asia/
• https://iscglobal.edu.vn/

Australia’s healthcare and medical device market is widely recognized as one of the most advanced, transparent, and high-value sectors in the Asia-Pacific region. However, this immense potential is matched by stringent technical barriers. To legally import, market, and distribute medical devices, pharmaceuticals, or health supplements in Australia, businesses must successfully navigate the rigorous approval process of the TGA.

The following article provides a comprehensive overview of the TGA, the major challenges businesses face, and our expert end-to-end consulting solutions.

1. WHAT IS THE TGA AND THE ARTG?

The TGA (Therapeutic Goods Administration) is Australia’s government authority responsible for regulating, evaluating, licensing, and monitoring therapeutic goods. Acting as the ultimate regulatory gatekeeper, the TGA ensures that all medical products supplied in Australia meet the highest standards of safety, quality, and performance.

Every product successfully approved by the TGA must be entered into the ARTG (Australian Register of Therapeutic Goods)—Australia’s national public database. Without an active ARTG entry, importing, advertising, or supplying your product in Australia is strictly illegal.

The TGA’s Regulatory Scope Includes:

• Medical Devices: From consumables (face masks, surgical drapes, syringes) to in-vitro diagnostics (IVDs), software as a medical device (SaMD), and active implantables.
• Medicines: Prescription drugs, over-the-counter (OTC) medicines, and vaccines.
• Complementary Medicines: Vitamins, minerals, herbal extracts, and dietary supplements.
• Biologicals: Human blood, tissues, and cell-based products.

2. RISK-BASED CLASSIFICATION OF MEDICAL DEVICES UNDER TGA

Unlike other jurisdictions, the TGA applies a highly detailed risk-classification framework that directly determines the application pathway, timeline, and cost. Medical devices are categorized into distinct risk classes:

• Class I (Low Risk): E.g., standard surgical face masks, bandages, non-invasive manual surgical instruments. Typically subject to a self-declaration pathway with fast processing times.
• Class IIa (Low-Medium Risk): E.g., hypodermic needles, surgical gloves, blood pressure monitors. Requires moderate technical file assessment.
• Class IIb (Medium-High Risk): E.g., ventilators, infusion pumps, condoms. Requires strict evaluation of clinical evidence and quality management systems.
• Class III & AIMD (High Risk & Active Implantable Devices): E.g., heart valves, pacemakers. Subject to the highest level of scrutiny, requiring extensive clinical data and direct TGA conformity assessment.

3. KEY BENEFITS OF OBTAINING TGA CERTIFICATION

• Gateway to Oceania: A mandatory prerequisite to participate in procurement tenders for both public and private hospital networks in Australia.
• Global Benchmark of Quality: The TGA is globally recognized for stringency comparable to the US FDA and European CE marking. Achieving TGA clearance serves as an ultimate testament to product quality and safety.
• Leverage for International Expansion: Many countries across Southeast Asia and Latin America streamline or expedite local registration pathways for products that already hold TGA or FDA approvals.

4. THE THREE MAJOR CHALLENGES FOR OVERSEAS MANUFACTURERS

Foreign manufacturers often incur heavy financial losses and delays due to the following hurdles:

1. The Australian Sponsor Requirement: Australian law mandates that only a local legal entity (an Australian Sponsor) can submit applications and hold the ARTG inclusion on behalf of overseas manufacturers. Finding a reliable, compliant Sponsor is a critical bottleneck.
2. Complex Technical Files and Quality Systems: The TGA imposes rigorous demands on Quality Management Systems (QMS). Even if a manufacturer holds ISO 13485 or CE certification, the TGA maintains unique, specific requirements regarding clinical evidence and safety warnings.
3. Strict Financials and Regulatory Pitfalls: A misclassified device or improperly filled application can result in immediate rejection, the forfeiture of non-refundable government fees (ranging from thousands to tens of thousands of AUD), and restarting the process from scratch.

5. ISC GLOBAL’S COMPREHENSIVE TGA CONSULTING SOLUTIONS

To help manufacturers overcome these complexities, ISC Global provides an end-to-end TGA consulting solution covering the entire product lifecycle across four core phases:

Phase 1: Assessment, Review & Strategic Planning

• Review product technical specifications and perform precise risk classification in accordance with Australian regulations.
• Conduct a Gap Analysis comparing existing documentation (ISO 13485, CE, FDA, clinical test reports) against TGA requirements.
• Provide a detailed cost and timeline estimate, outlining official government fees (TGA Fees & Charges) to ensure transparent financial planning.

Phase 2: Technical File Preparation & Standardization

• Guide and directly assist in drafting technical documentation, including the Declaration of Conformity, Risk Management Report, and Clinical Evaluation Reports.
• Review and standardize labeling and Instructions for Use (IFU) to ensure strict adherence to Australian medical warning guidelines.
• Advise on strengthening your QMS to prepare for potential regulatory audits.

Phase 3: Sponsor Connection & Dossier Submission

• Sponsor Solutions: Assist in connecting manufacturers with reputable, trusted Australian Sponsors, protecting your commercial interests and technical data confidentiality.
• Support the Sponsor in submitting and verifying Manufacturer Evidence.
• Manage the formal electronic submission process via the TGA’s electronic Business Services (eBS) portal.

Phase 4: Regulatory Liaison & Post-Market Maintenance

• Act as the direct liaison to handle and resolve any Requests for Information (RFIs) or inquiries from TGA evaluators within statutory timeframes.
• Successfully deliver the final ARTG certificate.
• Advise on post-market surveillance obligations and ongoing annual maintenance duties.

6. WHY PARTNER WITH ISC GLOBAL?

With deep expertise in international standards (ESG, ISO, risk management, and compliance), ISC Global approaches TGA certification not merely as a paperwork exercise, but as a strategic optimization of your core manufacturing process:

• Deep Technical Expertise: Our specialists understand intricate regulations, minimizing the risk of application rejections.
• Transparency & Accountability: Committed roadmaps with no hidden costs, supporting you all the way until your products successfully enter the Australian market.
• Global Network: Fast and dependable connections with certified Australian Sponsors.

Ready to Conquer the Billion-Dollar Australian Market? Do not let technical barriers slow down your commercial expansion. Contact ISC Global today to receive a complimentary preliminary risk-classification assessment!

Contact us to download the bilingual English-Vietnamese PDF standard: from only $50

On the path toward integration and export, correctly understanding and applying international standards is essential. Yet language and technical terminology often pose real barriers. We are pleased to introduce our bilingual (English – Vietnamese) standards documentation service, translated by our own team of certification consultants.

What We Provide

• A clause-by-clause bilingual comparison, easy to consult and file.

• Professional Vietnamese translation in correct technical terminology, ready to use.

• Interpretation notes and application guidance from hands-on experts.

• Fast delivery in editable, easy-to-store PDF/Word format.

Standards Covered

ISO management systems (9001, 14001, 45001, 37001); sustainability certifications (ISCC, FSC, VFCS/PEFC); textiles and recycled materials (GRS, OCS, OEKO-TEX); social responsibility and ESG (SMETA, EcoVadis, Fairtrade), and many other industry standards upon request.

Why Choose Us

Our documents are translated by professionals who directly consult on and audit certifications, so the translation is accurate not only in language but also in real-world application — saving you time and reducing errors when preparing documentation.

Pricing

From only USD 50 per document, depending on length and complexity. Please send us the standard name to receive a free, accurate quotation.

How to Order

1. Contact us with the name of the standard you need.

2. Receive a quotation and delivery time.

3. Make payment and receive your document by email.

Payment

Bank transfer via QR code (provided with the quotation), or via PayPal: ducluongservices@gmail.com.

We look forward to accompanying you on your certification journey.

Best regards,

CONTACT INFORMATION

Hotline: +84 933096426 – +84 868 591 260

Email:

• info@iscglobal.asia
• van.pham@iscglobal.asia

Website:

• https://iscglobal.asia/
• https://iscglobal.edu.vn/

The European Union (EU) market consistently leads the world with stringent standards designed to protect human health and the environment. Among these, the EU REACH Regulation (EC 1907/2006)—Registration, Evaluation, Authorisation and Restriction of Chemicals—is not merely a legal barrier, but has become a core benchmark for evaluating the competency of international suppliers.

For export-driven manufacturers, mastering REACH compliance ensures not only seamless customs clearance but also serves as a strategic stepping stone to elevate their sustainability ratings on global assessment platforms.

1. THE ESSENCE OF REACH AND THE PARADIGM SHIFT IN SUPPLY CHAIN RESPONSIBILITY

Unlike traditional chemical regulations, REACH operates on the fundamental principle of “No Data, No Market”. This creates a massive shift in responsibility: regulatory authorities are no longer tasked with proving a chemical is hazardous; instead, the burden of proof falls entirely on businesses (manufacturers and importers) to fund testing, gather data, and prove their products are safe.

This regulation impacts the entire manufacturing ecosystem:

• Basic Chemicals & Mixtures: Paints, solvents, printing inks, industrial adhesives, and wastewater treatment chemicals.
• Articles (Consumer & Industrial Goods): Products with a physical shape determining their function—ranging from wooden furniture, textiles, and footwear to electronic components, solar panels, and complex industrial machinery.

2. THE CORE TECHNICAL CHALLENGE: MANAGING “ARTICLES”

A major blind spot for many export businesses is the assumption: “We sell finished products, not chemicals, so REACH does not apply to us.” This is a critical misconception.

Under REACH, all articles are composed of chemicals and materials, and must therefore comply with stringent regulations:

• The O5A Rule (Once an Article, Always an Article): Following a landmark ruling by the European Court of Justice, the 0.1% weight by weight (w/w) threshold for Substances of Very High Concern (SVHCs) is not calculated based on the total weight of the finished product (e.g., a wooden table or an industrial machine). Instead, it applies to each individual component (e.g., the plywood adhesive, the surface coating, the plastic cable jacket, or a single galvanized screw).
• SCIP Database Notification: Since January 2021, any article containing SVHCs > 0.1% w/w must be declared—including its material structure and identification codes—to the ECHA SCIP database before being placed on the EU market.
• Restriction List (Annex XVII): Strict control of specific hazardous substances across industries. Examples include limits on Formaldehyde emissions in engineered wood, Phthalates in plastic components, or heavy metals (Lead, Cadmium, Chromium VI) in plated parts.

3. INTEGRATING REACH INTO ESG AND ECOVADIS STRATEGIES

As the push for sustainable development (Net Zero, ESG) accelerates, REACH compliance data should no longer be confined to the QA/QC department. It is a quantifiable asset that directly enhances a company’s corporate sustainability profile:

1. Synergy with EcoVadis Scoring:
   • In the Environment theme, having a robust chemical management process, lifecycle analysis, and a phase-out roadmap for SVHCs serves as compelling evidence to achieve an “Advanced” or “Outstanding” score.
   • In the Sustainable Procurement theme, establishing a supplier assessment process (controlling the Bill of Materials, demanding REACH compliance from subcontractors) is a mandatory requirement for large-scale enterprises.
2. Compatibility with ISO Management Systems: The Chemical Safety Assessment (CSA) data required by REACH provides perfect input for identifying environmental aspects and occupational health risks in ISO 14001 and ISO 45001 systems.
3. Supplier Selection Criteria: Global corporations now apply strict ESG filters when procuring equipment (from wastewater treatment plants to renewable energy systems). The ability to provide a transparent, REACH-compliant material profile represents an absolute competitive advantage.

4. THE COMPREHENSIVE REACH CONSULTING & COMPLIANCE ECOSYSTEM AT ISC GLOBAL

Understanding the technical barriers and the pressure to synchronize enterprise standards, ISC Global offers a holistic suite of solutions, partnering with businesses from the initial gap analysis to successful market entry:

4.1. Gap Analysis & Supply Chain Risk Assessment

• BOM (Bill of Materials) Teardown & Review: In-depth analysis of complex product material lists to accurately identify components at risk of containing SVHCs or restricted substances (Annex XVII).
• Supplier Auditing: Establishing forms, capability assessment procedures, and evidence requirements (REACH Declarations, Test Reports) for Tier 2 and Tier 3 raw material suppliers.
• Substitution Roadmap: Consulting on strategies to replace high-risk chemicals to meet green procurement standards.

4.2. In-depth Training & Internal Capacity Building

• Designing practical training modules tailored for the Board of Directors, Procurement, QA/QC, and EHS Engineering departments.
• Guidance on reading, validating, and authoring Safety Data Sheets (SDS) in accordance with the latest REACH structural standards.
• Training on methodologies to integrate chemical management into ISO 14001, ISO 45001, and optimizing responses for EcoVadis questionnaires.

4.3. Only Representative (OR) Services

• For companies directly supplying chemicals/mixtures, ISC Global connects with European partners to act as a legal Only Representative (OR).
• Empowering non-EU businesses to proactively handle ECHA Registration procedures, ensuring 100% confidentiality of commercial formulations without relying on a fixed EU importer.
• Holding an independent REACH certificate allows businesses to freely expand their customer network across the entire EU bloc.

4.4. ECHA Data Management & SCIP Notification

• Consulting on smart Testing Plans: Selecting the right testing parameters at international laboratories (SGS, Intertek, TUV, etc.) to optimize costs and eliminate unnecessary testing.
• Directly executing technical dossier creation on the IUCLID software and fulfilling SCIP Database notification obligations for complex articles.

Partner with ISC Global – Transforming technical barriers into a sustainable competitive advantage.

Complying with EU REACH does more than protect your goods from legal risks at the border; it proves that your risk management and sustainable development systems meet world-class standards.

Contact the expert team at ISC Global today to launch a pre-assessment project for your supply chain

Contact us to download the bilingual English-Vietnamese PDF standard: from only $50

On the path toward integration and export, correctly understanding and applying international standards is essential. Yet language and technical terminology often pose real barriers. We are pleased to introduce our bilingual (English – Vietnamese) standards documentation service, translated by our own team of certification consultants.

What We Provide

• A clause-by-clause bilingual comparison, easy to consult and file.

• Professional Vietnamese translation in correct technical terminology, ready to use.

• Interpretation notes and application guidance from hands-on experts.

• Fast delivery in editable, easy-to-store PDF/Word format.

Standards Covered

ISO management systems (9001, 14001, 45001, 37001); sustainability certifications (ISCC, FSC, VFCS/PEFC); textiles and recycled materials (GRS, OCS, OEKO-TEX); social responsibility and ESG (SMETA, EcoVadis, Fairtrade), and many other industry standards upon request.

Why Choose Us

Our documents are translated by professionals who directly consult on and audit certifications, so the translation is accurate not only in language but also in real-world application — saving you time and reducing errors when preparing documentation.

Pricing

From only USD 50 per document, depending on length and complexity. Please send us the standard name to receive a free, accurate quotation.

How to Order

1. Contact us with the name of the standard you need.

2. Receive a quotation and delivery time.

3. Make payment and receive your document by email.

Payment

Bank transfer via QR code (provided with the quotation), or via PayPal: ducluongservices@gmail.com.

We look forward to accompanying you on your certification journey.

Best regards,

CONTACT INFORMATION

Hotline: +84 933096426 – +84 868 591 260

Email:

• info@iscglobal.asia
• van.pham@iscglobal.asia

Website:

• https://iscglobal.asia/
• https://iscglobal.edu.vn/

Vietnam has become one of the world’s leading production hubs for hard-surface flooring — from engineered and laminate wood flooring to vinyl (LVT/SPC), quartz stone flooring, rubber flooring and flooring adhesives. As international buyers, green-building projects and retail chains increasingly demand independently verified low-emission products, FloorScore® certification has moved from a “nice-to-have” to a de facto market-entry requirement for many export contracts into North America and Europe.

This guide, prepared by ISC Global — an international standards and ESG certification consulting firm based in Ho Chi Minh City, Vietnam — explains what FloorScore® certification actually verifies, how the certification process works, and what Vietnamese manufacturers need to prepare, based on the current official programme documentation.

1. What Is FloorScore® Certification?

FloorScore® is the most widely recognised Indoor Air Quality (IAQ) certification programme for hard-surface flooring materials, flooring adhesives and underlayments. It was developed by SCS Global Services in conjunction with the Resilient Floor Covering Institute (RFCI), a leading US flooring-industry association. SCS Global Services is currently the programme’s exclusive certification body.

Unlike self-declared “eco-friendly” marketing claims, FloorScore® is a third-party, independently verified certification based on scientific emissions testing combined with an on-site factory audit — which is precisely why it carries commercial weight with sourcing and procurement teams that self-declared claims cannot match.

2. The Technical Basis: What Does FloorScore® Actually Measure?

Certified products must demonstrate compliance with volatile organic compound (VOC) emission limits under two key documents:

• SCS-105 Indoor Air Quality Standard, Version 4.2 (December 2023) — the current certification standard, with Appendix 1 setting out FloorScore®-specific requirements.
• CDPH/EHLB Standard Method V1.2 (January 2017), commonly known as California Section 01350 — the chamber-based test method modelling classroom and private-office exposure scenarios.

Under the current standard, the programme evaluates 35 individual VOCs, including formaldehyde. Certification is not based on a single test result alone; it also requires formulation review, factory document control, an on-site audit, representative “worst-case” sample selection, and independent technical review before a certification decision is issued.

3. Why FloorScore® Matters for Manufacturers Right Now

Vietnam’s wood and wood-product export sector has continued to post strong growth, with wood and wood-product exports reaching roughly USD 15.5 billion over the first eleven months of a recent reporting year — while global buyers increasingly favour “greener,” independently verified building materials over commodity products. Industry research on the regional laminate flooring market also points to a marked rise in environmental awareness among buyers over the past several years, with manufacturers holding low-VOC or sustainability certifications reporting notably faster sales growth than uncertified competitors. At the same time, Vietnam’s own green building materials market is projected to expand at a high single-digit compound annual growth rate through the next decade, driven by urbanisation and the country’s Net Zero policy direction.

For Vietnamese manufacturers, this translates into three concrete commercial advantages from holding FloorScore® certification:

• De facto entry requirement for many North American and European flooring distributors and retail chains
• Green-building credit contribution: FloorScore®-certified products are recognised under major international green-building rating systems, including LEED v4.1, the WELL Building Standard, BREEAM, CHPS and Green Globes — making certified products easier to specify into green construction projects
• Durable brand asset: certified products are listed in the public SCS Green Products Guide, building long-term trust with B2B buyers and specifiers

4. Product Scope

FloorScore® applies to most categories of hard-surface flooring and related products, including:

• Laminate and engineered wood flooring
• Vinyl sheet/roll flooring, LVT, SPC and WPC flooring
• Quartz stone flooring
• Rubber flooring and linoleum
• Hard-surface carpet tile meeting the applicable criteria
• Flooring adhesives and underlayments

5. What FloorScore® Confirms — and What It Does Not

This is a frequent point of confusion for first-time applicants: FloorScore® only evaluates VOC emissions and manufacturing consistency related to emissions. It does not evaluate mechanical durability, slip resistance, fire resistance, colour fastness or water resistance. Manufacturers needing to substantiate those performance claims must pursue separate testing under the relevant standards (for example, ASTM methods for slip or abrasion resistance).

6. The Certification Process, Step by Step

According to SCS’s published guidance, the average certification cycle takes about three months from a signed work order to a final decision, with VOC testing itself typically taking 3–4 weeks. In practice, total project duration — from kick-off to decision — commonly runs 12–14 weeks, depending on documentation readiness and auditor/laboratory scheduling.

7. What Manufacturers Need to Prepare

• A complete list of models/SKUs intended for the certificate, including trade names, thickness, dimensions and target markets
• Formulation/construction data, Bill of Materials, and SDS/TDS documentation for raw materials and coatings
• A manufacturing process flow diagram and identification of VOC-relevant process control points
• A Quality Control Plan or equivalent documentation covering traceability, change control and nonconforming-product handling
• Corporate and OEM-relationship documentation where a brand owner and contract manufacturer are separate legal entities

8. The Role of a Local Consulting and Coordination Partner

Given the complexity of formulation review, worst-case sample selection and factory-level documentation requirements, most first-time applicants benefit substantially from working with an experienced local consulting partner. A well-structured engagement typically separates two distinct roles to preserve the programme’s impartiality principle:

• A technical consulting partner (in Vietnam, typically an ISO/ESG consulting firm) that delivers training, performs the gap assessment, and helps build the technical dossier and Quality Control Plan
• A local contracting and coordination partner that signs the domestic coordination contract, issues local invoices, and manages communication and scheduling with the certification body and testing laboratory

Crucially, neither party performs the audit, sampling, testing, or certification decision — those functions remain the independent authority of SCS Global Services and the accepted testing laboratory. This separation of roles is what protects the credibility of the resulting certificate in the eyes of international buyers.

9. Frequently Asked Questions

Is FloorScore® a legal requirement in Vietnam? No. FloorScore® is a voluntary, market-driven certification rather than a Vietnamese regulatory requirement. However, it is frequently a contractual requirement imposed by North American and European importers and distributors.

How long does FloorScore® certification remain valid? Certification must be maintained on the programme’s ongoing cycle, which includes periodic desk reviews and may require re-testing as determined by SCS.

Can a brand owner and a contract manufacturer (OEM) share one certificate? SCS will confirm the appropriate certification structure based on the actual contractual and ownership relationship between the brand owner and the manufacturing site.

What is the typical cost structure for FloorScore® certification? Costs generally fall into three categories: (i) technical consulting and training fees, (ii) local contracting/coordination fees, and (iii) fees paid directly to the certification body, auditor and testing laboratory under their own official quotations.

Get Expert Support for FloorScore® Certification in Vietnam

ISC Global supports Vietnamese flooring manufacturers throughout the full FloorScore® certification journey — from staff training and gap assessment to technical dossier preparation and coordination support with the certification body.

Contact us for business consultation:

Hotline: +84 933 096 426 – +84 868 591 260

Email: info@iscglobal.asia | van.pham@iscglobal.asia

Website: iscglobal.asia | iscglobal.edu.vn