
European Chemicals Agency
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The European Chemicals Agency (ECHA)
The European Chemicals Agency (ECHA) is responsible for implementing the EU’s chemicals legislation to ensure the safe use of chemicals. Its main roles include:
- Regulation Implementation
ECHA manages and helps companies comply with specific EU legislation on chemicals or biocides: - Chemical Safety
The agency evaluates the properties and hazards of chemical substances, ensuring that companies comply with safety standards. ECHA works with the European Commission and EU governments to identify substances that give cause for concern and take decisions on EU-level risk management. - Data Management
ECHA smaintain databases necessary for the REACH system, coordinating the in-depth evaluation of information provided on chemicals. - Public Information
ECHA provides information on chemicals and their safe use through a unique free database.
ECHA supports the validation and use of New Approach Methodologies (NAMs) through several initiatives:
- Guidance and Communication
ECHA provides extensive guidance and communicates with registrants to promote the use of NAMs and alternative methods to animal testing. - Funding and Collaboration
The agency funds activities such as the OECD QSAR Toolbox and collaborates with research institutions and industry stakeholders to develop and validate NAMs. - Workshops and Case Studies
ECHA organizes scientific workshops and conducts case studies to explore the application of NAMs in regulatory contexts, such as hazard assessment and read-across strategies. - Regulatory Acceptance
ECHA works towards the regulatory acceptance of NAMs by providing clear guidelines and frameworks, such as the Read-Across Assessment Framework (RAAF), to ensure that NAMs are scientifically robust and reliable.
National helpdesks
National helpdesks have been established as a first point of contact for questions about the Biocides Regulation, the Regulation on Classification, Labeling and Packaging and REACH (Regulation on Registration, Evaluation, Authorization and Restriction of Chemicals). They can give you advice in your own language and are aware of local conditions that may be important for proper compliance with these regulations.
ECHA and the national helpdesks work together to provide support to companies on the REACH, CLP and Biocidal Products regulations.
See the table below to see who can best help you with your query.
National helpdesks
Contact your national helpdesk on the following questions
ECHA
Contact us on the following questions:
REACH and CLP
- Regulatory and scientific questions from EU and non-EU companies on REACH, CLP (including poison center notifications (PCN))
REACH and CLP
- REACH and CLP submission and process
- Evaluation
- Ongoing disputes and pending litigation
- Annex XV SVHC dossiers (or RoI) proposed by ECHA or Commission
- Complex borderline cases of substance in articles
- ECHA’s fees and charges
- Questions that require harmonisation and consultation with the European Commission
- Other policy related questions
BPR
- Active substance approval – dossier evaluation
- Annex I inclusion
- National authorisation
- Mutual recognition
- Simplified authorisation
- Same biocidal product authorisation
- Parallel trade
- Treated articles
- National laws
- Classification, labelling and packaging of biocidal products
- National fees
- Enforcement
- Scope questions – including Art 3(3) requests
BPR
- Active substance approval – peer review
- Article 95
- Review Programme
- Data sharing and inquiry
- Classification & labelling of active substances
- Union authorisation
- Technical equivalence
- ECHA's fees
- ECHA's guidance
The NAM Navigator was commissioned by TPI under the direction of the More Knowledge with Fewer Animals program of ZonMw.
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