Contact Information

Headquarters:
Vuorikatu 14 B
00100 Helsinki, Finland.
Tel: +358 (0) 9 412 3055
Fax: +358 (0) 9 412 3049
Email: sales@reachlaw.fi

Delhi Office:
REACHLaw India Private Ltd (A subsidiary of REACHLaw Ltd., Finland)
Unit 410,411,412 & 431, Fourth Floor, City Centre Mall, Sector-12, Dwarka, New Delhi-110075. India
Tel: +91 11 4011 4748
Email: contact@reachlaw.co.in

Contact us

EU REACH Compliance Services for Indian Manufacturers, Formulators and Merchant Exporters


Helping Indian manufacturers and exporters of chemicals, polymers, mixtures and articles achieve uninterrupted access to the EU/EEA market with confidence and regulatory clarity.

Our India-based REACH specialists provide technical and regulatory support, while our EU headquarters acts as your Only Representative (OR) in accordance with EU REACH Regulation (EC) No 1907/2006.

We deliver end-to-end REACH compliance support, including Exemption Assessment, Substance Identification, REACH Registration, Only Representation, Safety Data Sheets, IUCLID Dossiers, REACH Supplier Due Diligence, REACH Out-tasking, REACH Audits, Testing Support, SVHC Compliance, SCIP, Evaluations, Restriction and Authorisation Services.

REACH regulatory specialists based in India (New Delhi and Mumbai)
EU Headquarters serving as your legal Only Representative for REACH compliance
Integrated India-EU compliance support across the full REACH lifecycle
Understanding EU REACH

What Indian manufacturers and exporters need to know

The EU REACH Regulation (EC No 1907/2006) is the central EU law governing chemicals placed on the European market. It applies to substances on their own, in mixtures and, in certain cases, in articles imported into the EU/EEA in quantities of at least 1 tonne per year, unless exempted from REACH registration requirements.

Indian based companies are outside the EU/EEA market, therefore, the direct registration obligation normally sits with the EU importer. However, an Indian manufacturer or formulator can appoint an EU/EEA-based Only Representative (OR) to take over those importer duties under Article 8 of REACH, simplifying EU market access, maintaining commercial independence, and protecting confidential business information from EU importers.

"No data, no market" — substances requiring REACH registration must have a valid registration before being placed on the EU/EEA market.

R

Registration

Substances at or above 1 tonne/year must be registered with ECHA via REACH-IT using an IUCLID dossier, with required hazard and use data.

E

Evaluation

ECHA and Member State authorities assess dossiers and substances for compliance and risk (dossier evaluation, CoRAP, substance evaluation).

A

Authorisation

SVHCs on Annex XIV require authorisation before continued use beyond the sunset date. Applications submitted to ECHA.

R

Restriction

Annex XVII restricts or bans specific substances and uses. It requires expert assessment of conditions before you draw any compliance statement for your products.

What we do

EU REACH Services for Indian Exporters

We provide the full spectrum of REACH compliance services tailored for Indian manufacturers, formulators, article producers, traders, and exporters. REACHLaw supports Indian companies with EU REACH and CLP compliance for market access to the EU/EEA. Our services cover registration, Only Representative support, dossier preparation, data sharing, evaluation, authorisation, restriction, and related supply chain compliance requirements.

1. REACH Exemption Assessment

1. REACH Exemption Assessment

Systematic assessment of whether your product, substance or use may fall outside REACH registration obligations as defined under REACH Article 2. Covers re-imports, polymers, intermediates, Annex IV, V exemptions, PPORD (product and process orientated research and development), recovered substances and low-volume situations. A documented professional opinion supported by ECHA guidance, and if required, we will also seek input from relevant consortia or authorities, such as Member State Competent Authorities.
2. Only Representative (OR) Services

2. Only Representative (OR) Services

REACHLaw provides reliable Only Representative services as a member of the Only Representative Organization (ORO), supporting non-EU/EEA manufacturers and formulators under Article 8 of the EU REACH Regulation.

Our OR services cover non-EU/EEA manufacturers, formulators and article producers exporting to the EU/EEA, ensuring regulatory compliance and market access.

We also provide support services for Indian companies that appoint their own EU-based subsidiary as Only Representative, including regulatory guidance, documentation support and compliance assistance.

In addition, we offer Only Representative transfer (OR change) support services to ensure a smooth and compliant transition.

3. REACH Inquiry

3. REACH Inquiry

Support for preparing REACH inquiry dossiers and reviewing substance identity, 12-year data rule applicability, and communication with the lead registrant to prepare an accurate budget for member registration covering future costs before registration. Companies planning to register a substance must inquire whether a registration has already been submitted, and substance identity information must be complete and clear.
4. Testing Strategy and Study Support

4. Testing Strategy and Study Support

Support to assess available data, identify information gaps and plan additional testing where required. We help identify and recruit reliable OECD GLP laboratories from India and internationally to fulfil testing requirements, including study monitoring.

5. REACH Registration and Co-registration

5. REACH Registration and Co-registration

We provide end-to-end support for REACH registration as co-registrant or Lead Registrant*, including substance identification, registration strategy, testing support, data sharing, Letter of Access negotiations, IUCLID dossier preparation, joint submission and REACH-IT related support. We assist companies with co-registrant (or member registration) and Lead Registrant registrations.

*REACHLaw's Lead Registration Process

When you take the lead role in a registration, REACHLaw handles the administrative and technical burdens to guarantee dossier completeness. Our expert team manages:

  • Data gap analysis, testing & chemical safety assessment: Identifying existing data, determining what testing is required, and completing hazard, PBT, exposure assessments and risk characterization
  • Dossier compilation: Populating IUCLID datasets and drafting the Chemical Safety Report (CSR)
  • Data sharing & consortium management: Facilitating Joint submission communication, legal drafting of data sharing agreements, itemised LoA calculations and handling financial transactions
  • Dossier submission: Submitting the technical dossier and CSR to ECHA
  • Post-submission: Managing Letters of Access (LoA) sales and ensuring continuous compliance using project management service
6. Data Sharing, LoA and Consortium Support

6. Data Sharing, LoA and Consortium Support

Support with data-sharing discussions, Letter of Access review, cost-sharing considerations and consortium or joint submission management. REACHLaw provides consortium management as part of its REACH & CLP services.

7. IUCLID Dossier Preparation and Review / Technical Dossier & Chemical Safety Report Conformity Assessment

7. IUCLID Dossier Preparation and Review / Technical Dossier & Chemical Safety Report Conformity Assessment

Preparation of REACH registration dossiers in IUCLID 6 for submission through REACH-IT, including technical completeness checks, endpoint review, data waiving justifications, classification review, use information, guidance on safe use and update strategies.

Our service includes review of current technical dossiers and chemical safety reports for REACH registration, dossier updates and maintaining your dossier healthy and fit.

We also offer conformity assessment of your existing technical dossier and chemical safety report for both lead and member registration dossiers and check those for gaps and undertake required update services ahead of ECHA compliance checks or evaluation decisions.

8. Chemical Safety Assessment (CSA) and Chemical Safety Report (CSR)

8. Chemical Safety Assessment (CSA) and Chemical Safety Report (CSR)

Preparation and review of Chemical Safety Assessments and Chemical Safety Reports for substances requiring registration above 10 tpa. Includes hazard assessment, PBT/vPvB screening, exposure assessment, risk characterisation and exposure scenario development using CHESAR.

9. SDS and eSDS Review

9. SDS and eSDS Review

Safety Data Sheet review and preparation against REACH Annex II and CLP requirements. Extended SDS (eSDS) review covering exposure scenarios, operational conditions and risk management measures. We check CLP classification consistency, labelling accuracy and downstream user communication obligations.

10. SVHC, Candidate List and SCIP Support

10. SVHC, Candidate List and SCIP Support

Screening of substances and articles against the SVHC Candidate List. Advice on supply chain communication obligations, SCIP database notification for articles containing SVHCs above 0.1% w/w, and monitoring Candidate List updates yearly that may affect your products.

More information on REACHLaw SVHC Support services → Circular Economy Services →
11. Dossier and Substance Evaluation Support

11. Dossier and Substance Evaluation Support

Assistance responding to ECHA compliance check (CCH) decisions, dossier evaluation letters, CoRAP substance evaluation decisions and testing proposals. We help draft technically sound responses, identify and recruit reliable OECD GLP laboratories from India to fulfil testing requirements including study monitoring, update technical dossiers and chemical safety reports, and comply with ECHA deadlines.

12. Substance, Nano and Polymer Identification

12. Substance, Nano and Polymer Identification

Expert assistance in correctly identifying your substance, nano material or polymer for REACH purposes — including boundary composition, impurity profile, CAS/EC number confirmation, mono-constituent vs. multi-constituent, UVCB characterisation and polymer monomer assessment. Critical for dossier quality and avoiding evaluation issues.

13. Authorisation and Restriction Strategy

13. Authorisation and Restriction Strategy

Business impact assessment for Annex XIV (Authorisation List) and Annex XVII (Restriction). Support for authorisation applications, substitution analysis, socio-economic assessment and restriction compliance review for substances of very high concern.

REACHLaw Authorisation Services → REACH Restriction Services →
14. REACH Audit and Compliance Review

14. REACH Audit and Compliance Review

Structured audit of your REACH compliance status covering substance identity, OR Article 8 compliance, registration dossier (FULL or Intermediate), strictly controlled conditions, chemical safety report, SDS, eSDS, dossier updates (Article 22), downstream user obligations, SVHC, authorisation and restriction — identifying gaps and prioritising corrective actions with a practical roadmap before actual audit by MSCA.

We offer both mock audit and on-site support to assist your team with actual audits with inspectors from start to closure of the inspection.

15. REACH Dossier Update Tracking and Maintenance (Article 22 Support)

15. REACH Dossier Update Tracking and Maintenance (Article 22 Support)

REACH registration is not a one-time compliance activity. Registrants must keep their dossiers up to date when relevant information changes. REACHLaw supports routine monitoring of dossier update triggers, tracking of Article 22-related update needs, coordination with co-registrants or Lead Registrants, and preparation or review of required dossier updates. Our IT support allows companies to demonstrate needed processes, systems and alerts to identify when changes to a registration are required. We also offer IT support service for volume tracking for both direct and indirect imports.

Typical support includes:

  • Tracking Article 22 dossier update triggers
  • Monitoring tonnage, composition, use and classification changes
  • Reviewing supplier and customer feedback that may affect the registration
  • Checking whether new data, SDS/eSDS or CSR updates are needed
  • Coordinating with Lead Registrant, co-registrants or consortium
  • Supporting IUCLID dossier updates and REACH-IT submission planning
  • Monitoring evaluation decisions and update deadlines
  • Maintaining records to support enforcement readiness
16. REACH Training and Capacity Building

16. REACH Training and Capacity Building

Practical REACH training for regulatory affairs, R&D, export compliance, QA, EHS and product stewardship teams in India. Available online or at your facility. Please refer and enrol your team for the 3 days online EU REACH professional certificate course. You can find more information here.

Not sure whether your product requires REACH registration? Share your SDS or product details, uses in EU/EEA. Alternatively you can submit a filled template along with the product SDS for a no-obligation initial assessment.

🗎 Download our Substance Information Template for REACH registration and submit it to contact@reachlaw.co.in

Request an Assessment

REACH Supplier Due Diligence Services for EU Market Sourcing

REACHLaw supports EU importers, e-commerce players, formulators, polymer manufacturers, Indian traders and sourcing teams that procure products from Indian manufacturers/suppliers for the EU/EEA market. To support enforcement readiness and reduce supply-chain compliance risk, REACHLaw helps EU importers, e-commerce platforms and sourcing teams assess whether Indian suppliers can provide the REACH-related information required for EU market access.

Before you source from India, check REACH readiness. Our supplier due diligence service helps buyers and suppliers build a documented REACH compliance position to support EU market access and enforcement readiness.

Supplier REACH Due Diligence

Supplier REACH Due Diligence

Assessment of Indian suppliers before onboarding for EU-bound products. Includes review of product type, role in the supply chain, SDS availability, SVHC information, restriction risks, OR registration tonnage coverage and supplier REACH statements or declarations.

REACH Supplier Qualification Support

REACH Supplier Qualification Support

Support for buying teams to identify and shortlist suppliers that can provide appropriate REACH, CLP and supply-chain compliance documentation. Useful for EU importers looking for more reliable REACH-compliant suppliers from India.

Product Compliance Screening Before EU Import

Product Compliance Screening Before EU Import

Screening of substances, mixtures or articles against key REACH obligations before sourcing or shipment. Before import, we help assess whether the product may trigger REACH registration, SVHC communication, SDS, restriction or other supply-chain obligations.

SDS and Supply-Chain Documentation Review

SDS and Supply-Chain Documentation Review

Review of SDS, eSDS, product declarations and supplier compliance statements. We review supplier SDSs and related documentation to identify gaps, inconsistencies or missing REACH/CLP information before products are supplied to the EU market.

SVHC and Article Communication Support

SVHC and Article Communication Support

Support for article suppliers and EU buyers on Candidate List substance communication. We assist with SVHC screening and communication support for articles sourced from Indian suppliers and destined for EU customers. SVHC Support services →

REACH Restriction Compliance Review

REACH Restriction Compliance Review

Review of whether products may be affected by REACH Annex XVII restrictions, including relevant product categories and restricted substances. We help buyers and suppliers check whether EU REACH restriction requirements may affect products before export or import. Restriction services →

OR and Registration Route Assessment

OR and Registration Route Assessment

Assessment of whether the Indian supplier, EU importer or an Only Representative should manage REACH registration obligations. We help clarify whether REACH registration should be handled by the EU importer or through an Only Representative arrangement, including trustee services and volume record keeping/tracking services.

Supplier Corrective Action Plan

Supplier Corrective Action Plan

Where gaps are identified, REACHLaw helps the supplier improve documentation, assess registration needs, update SDS information, prepare declarations, check for exemptions or initiate registration-related actions as OR.

REACH Training for Suppliers and Buying Teams

REACH Training for Suppliers and Buying Teams

Short practical training for Indian suppliers, EU buying teams and e-commerce compliance teams on REACH basics, SDS, SVHC, restrictions, importer responsibilities and supplier documentation expectations. We train suppliers and sourcing teams to understand REACH expectations and improve the quality of compliance information exchanged across the supply chain.

Free Quick Consulting

Need REACH clarity before committing to a full project?

Book a free 30-minute consultation with a REACHLaw India expert for focused guidance on your immediate regulatory question. Suitable for Indian chemical exporters, manufacturers, formulators, merchant exporters, traders and product compliance teams at any stage.

  • How do I register a substance or mixture under REACH?
  • How do I change my current Only Representative?
  • I am a merchant exporter (non-EU based trader) — how can I register under REACH?
  • How do I correctly identify my substance or polymer for REACH?
  • I am a formulator — how do I register under REACH, or how to reduce cost of compliance by using supplier REACH registrations for all ingredients?
  • What is the 12-year data rule under REACH?
  • How to track volumes and customer information for direct and indirect imports into Europe?
  • Is my REACH IUCLID dossier and CSR compliant?
  • How much does EU REACH registration cost?
  • Does REACH apply to my product — substance, mixture, polymer, intermediate or article?
  • How to obtain a "REACH certificate", or what proof should I provide to my EU buyer?
  • Is my substance, polymer, intermediate or use exempt from REACH registration?
  • Should I appoint an Only Representative or rely on my EU importer?
  • How do I check whether my SDS is suitable for EU export?
  • Do I need an SDS, eSDS, CSR or exposure scenario?
  • What are my SVHC, SCIP, restriction or authorisation obligations?
  • Is my product affected by REACH Annex XVII restrictions?
  • How to obtain and purchase a Letter of Access?
  • What should I do if ECHA has sent a dossier or substance evaluation letter or draft decision?
  • When do I need to update my REACH registration dossier under Article 22?
  • I am an EU importer, formulator or e-commerce buyer sourcing from India — how do I qualify REACH compliant suppliers?
Book Your Free REACH Consultation
Our consultant will respond and contact you to fix a meeting.

This is a free 30-minute consultation. No commitment required. Paid extended advisory sessions are also available.

Who we work with

Industries We Serve

REACHLaw supports Indian exporters across a wide range of chemical-using and chemical-producing sectors. If your industry exports products to the EU/EEA, REACH obligations may apply to your substances, mixtures, or articles.

Chemicals & Raw Materials
Speciality Chemicals Petrochemicals Agrochemicals Fertilizers Solvents Base Oils Intermediates Minerals Metals Essential Oils Castor Derivatives Fatty Acids Oils & Bio-based
Polymers, Plastics & Rubber
Polymers Bio-polymers Monomers Plastics Plasticizers Rubber Resins Flame Retardants Packaging
Coatings, Adhesives & Formulations
Paints Coatings Inks Adhesives Sealants Lubricants Surfactants Formulations Cleansers
Consumer & Life Sciences
Cosmetics Pharmaceutical Flavours Fragrances Dyes Pigments Leather Textiles Gem & Jewellery
Industrial & End-Use Sectors
Automotive Tyres Aerospace & Defence Electronics Semiconductors Batteries Electrical & Telecom Equipment Medical Devices Engineering Toys Handicrafts Mobiles & Telecom
Circular Economy & Waste
Waste Management Recycling Recovered Substances Packaging Recyclers Bio-based Materials
Not sure if REACH applies to your sector? REACH obligations depend on product type (substance, mixture or article), role in the supply chain and EU/EEA tonnage — not on the industry label. Book a free consultation and we will assess your specific situation.
Frequently Asked Questions

EU REACH FAQ for Indian Exporters

Authoritative answers to the most searched REACH questions from Indian companies, covering registration, Only Representative, SDS, IUCLID, polymers, SVHC, dossier, and substance evaluation.

EU REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals — Regulation EC No 1907/2006) is the main EU law for chemicals. It applies to substances on their own, in mixtures and, in certain cases, in articles. Indian companies are outside the EU/EEA so the direct registration obligation normally sits with the EU importer. However, Indian exporters are commercially affected because EU customers routinely require REACH registration, SDS, SVHC information, substance identity confirmation or compliance proof before purchasing. Understanding your obligations — and your options — is the first step.
A company outside the EU/EEA cannot submit a REACH registration as an EU registrant directly. However, a non-EEA manufacturer may appoint an EEA-based Only Representative (OR) to take over the importer's registration duties and legal responsibilities under REACH. The OR submits and maintains the registration dossier on behalf of the non-EU manufacturer and is the point of legal contact with ECHA and MSCA. Indian manufacturers who export to the EU through multiple importers particularly benefit from this arrangement.
An Only Representative (OR) is an EEA-established legal entity appointed by a non-EEA manufacturer under Article 8 of REACH to fulfil importer obligations. The OR registers the substance, maintains the registration, manages the list of importers covered and communicates with ECHA. Appointing an OR simplifies EU market access, allows the Indian manufacturer to control registration and use information, reduces the burden on multiple EU importers and protects confidential formulation or composition data. ECHA confirms that an OR must be established in the EEA and have sufficient knowledge of the practical handling of the substance and information relating to it.
REACH registration is generally required when a substance is manufactured in or imported into the EU/EEA at one tonne or more per registrant per year, unless an exemption applies. The quantity is assessed per legal entity (the registrant or their OR), not across all importers combined. Below one tonne, registration is generally not required — but other obligations such as restrictions, authorisation, SDS, CLP, SVHC communication and article notification may still apply. Indian exporters should assess substance identity, product type, EU importer tonnage, OR appointment and possible exemptions before drawing conclusions.
Polymers themselves are currently not subject to registration under REACH, provided they meet the polymer definition under REACH. However, the monomers and other substances used in making the polymer may require registration if not already registered — this is known as monomer registration. Indian polymer exporters should not assume exemption without a professional assessment. The supplier's monomer registration alone is not sufficient to demonstrate that your product is REACH compliant.
Intermediates are not automatically outside REACH. They may qualify for specific registration provisions depending on whether they are non-isolated intermediates, on-site isolated intermediates or transported isolated intermediates, and whether strictly controlled conditions (SCC) are met. ECHA has dedicated guidance on intermediates describing when and how specific reduced-data provisions for intermediate registration can be used. An incorrect intermediate claim is a common dossier evaluation finding, so professional assessment is important before relying on intermediate status.
REACH requires that registrants of the same substance register jointly. The lead registrant submits the joint dossier containing shared data (hazard, classification, guidance on safe use). A Letter of Access (LoA) is the contractual mechanism that grants a registrant the right to refer to specific data owned by another party submitted in the joint dossier. Indian exporters working through an OR typically need to join an existing joint submission, assess LoA options and submit a co-registration dossier. REACHLaw can support the entire data-sharing negotiation and co-registration process.
IUCLID (International Uniform Chemical Information Database) is the software used to create, manage and submit REACH dossiers. Registration dossiers are prepared in IUCLID 6 and submitted through REACH-IT to ECHA. REACH-IT is ECHA's secure online system used for all REACH submissions — including inquiry, registration dossier submission, classification and labelling notification and communication with ECHA. Both tools require specialist expertise for correct and compliant dossier preparation. REACHLaw manages IUCLID and REACH-IT on behalf of clients.
Dossier evaluation is an ECHA process to check whether registration dossiers comply with information requirements. ECHA may issue a compliance check (CCH) decision requiring additional data or justifications within a set deadline. Substance evaluation is a separate process where Member State competent authorities assess whether a substance may pose risks to human health or the environment. CoRAP (Community Rolling Action Plan) lists substances selected for substance evaluation. If your substance is on CoRAP, you should monitor the timeline, review dossier quality and prepare for possible information requests. Both types of evaluation require timely, technically robust responses to ECHA.
A Safety Data Sheet (SDS) communicates hazard, safe handling, storage, exposure control and emergency information for a substance or mixture through the supply chain. Under REACH, an SDS must be provided for hazardous substances and mixtures and for substances on the Candidate List. An extended SDS (eSDS) includes exposure scenarios as an annex — required where a Chemical Safety Assessment has been carried out and exposure scenarios have been developed. The eSDS must be communicated to downstream users so they can verify that their uses are covered. Both SDS and eSDS must be updated without delay when new hazard, risk management or regulatory information becomes available.
SVHC (Substance of Very High Concern) is a substance with serious effects such as CMR properties, PBT/vPvB behaviour or endocrine disruption. SVHCs are added to ECHA's Candidate List, which is updated a few times a year (usually twice a year). If an article contains a Candidate List substance above 0.1% w/w, the supplier must communicate this to customers and consumers on request. SCIP is the ECHA database for articles containing SVHCs — EU-based article producers and importers must notify ECHA about such articles under the Waste Framework Directive. Indian exporters of articles to EU customers may be asked by their customers to provide SVHC data and support SCIP compliance.
Authorisation under REACH (Annex XIV) applies to certain substances of very high concern. Companies must obtain authorisation from ECHA to continue using or placing such substances on the EU market after a specified sunset date, unless an exemption applies. Restriction under REACH (Annex XVII) imposes conditions, limitations or bans on specific substances. It requires expert assessment of conditions before drawing any compliance statement for your products. Both instruments may affect Indian exporters whose products contain or use regulated substances.
CHESAR (Chemical Safety Assessment and Reporting tool) is an ECHA tool used by registrants to conduct chemical safety assessments and prepare Chemical Safety Reports. It structures the assessment of substance hazards, exposure and risk for different use scenarios and generates exposure scenarios for the eSDS. CHESAR is particularly relevant for registrations above 10 tpa where a CSR is required. REACHLaw uses CHESAR as part of its CSA/CSR preparation services for Indian exporters.
Costs depend on substance identity and complexity, tonnage band, existing registration status at ECHA CHEM, Letter of Access cost and the 12-year data rule, data gaps, testing charges, CSR requirement (above 10 tpa), classification, evaluation status, OR service scope and dossier preparation effort. ECHA also charges administrative fees that vary by tonnage band and company size (SME fee reductions apply). A REACHLaw quick consultation can help estimate a realistic budget and identify the most cost-effective path for your specific situation.
Changing your OR requires careful planning. The original OR must transfer all registrations, notifications and REACH-IT assets to the newly appointed OR. ECHA charges a fee for the OR identity change, which the new OR pays on behalf of the non-EEA manufacturer. After the transfer, relevant stakeholders including consortia, EU importers and downstream users must be informed. In some cases, a dossier update in REACH-IT is also required. REACHLaw handles OR transitions as a structured process to avoid compliance gaps and ensure continuity of EU market access.
ECHA CHEM is ECHA's public chemicals database, launched in 2024, which makes regulatory information on registered substances publicly available. It is useful for checking registration status, number of registrations, the 12-year data rule, names of registrants, type of substance, classification, evaluation status, restriction list, authorisation list, DWD notification and Candidate List substances, but it does not replace a company-specific compliance assessment. REACH-IT is the secure submission and communication portal used by registrants, ORs and notifiers to interact with ECHA for all formal submissions including registration dossiers, inquiry, dossier updates and authorisation applications.
Not finding your answer? Ask our experts →

A comprehensive EU REACH FAQ hub for Indian exporters covering 40+ questions on registration, OR, SDS, IUCLID, polymers, SVHC, authorisation, restriction, nano, microplastics, SCIP and ECHA evaluation is coming soon.

REACH registration India EU REACH consultant India Only Representative REACH REACH certification India IUCLID dossier preparation SDS eSDS review India SVHC compliance SCIP notification ECHA evaluation support REACH exemption assessment polymer REACH registration co-registration REACH Letter of Access REACH chemical safety report India CSR REACH REACH-IT ECHA CHEM downstream user obligations REACH dossier review substance identification REACH CoRAP substance evaluation REACH audit India CLP SDS India CHESAR CSA REACH compliance Indian exporters merchant exporter REACH REACH intermediate exemption REACH microplastics REACH nano materials PCN UFI CLP India authorization restriction SVHC lead registration member registration opt-out REACH REACH inquiry SIEF REACH supplier due diligence REACH out-tasking Article 22 dossier update REACH testing support India 12 year data rule REACH REACH volume tracking

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