Skip to Content
An agency of the European Union European Union Flag
  • Sign In
  • Quick Tools
    • Newsletter
    • Chemicals In Our Life
    • Poison Centres
    • CHESAR
    • EUON
    • IUCLID 6
ECHA
  • About Us
  • Contact
  • Jobs
  • Legislation
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals

      REACH regulation aims to improve the protection of human health and the environment from the risks that can be posed by chemicals.

      • Understanding REACH
      • Legislation
      • Substance identification
      • Communication in the supply chain
      • Use maps templates
      • Safety data sheets
      • Candidate List substances in articles

      Registration

      • Basics of registration
      • Research and development (PPORD)
      • Data sharing
      • Information requirements
      • Publishing information from dossiers
      • Registration statistics

      Evaluation

      • Basics of evaluation
      • Evaluation process
      • Examination of testing proposals
      • Compliance checks
      • Substance Evaluation
      • Progress in evaluation

      Authorisation

      • Authorisation process
      • Substances of very high concern identification
      • Recommendation for the Authorisation List
      • Applications for authorisation

      Restriction

      • Basics of restriction 
      • Restriction procedure
      • ECHA’s activities on restrictions
      • Preparation of a restriction proposal
      • Public consultations
      • Information on restricted substances
      Addressing substances of concern
      Appeals
      EUCLEF EUCLEF
      • Getting started with EU chemicals legislation
      • Nanomaterials
      • Substitution to safer chemicals
      • Appeals
      • Enforcement
      • Directors' Contact Group
    • CLP Classification, Labelling and Packaging

      The CLP Regulation ensures that the hazards presented by chemicals are clearly communicated to workers and consumers in the European Union through classification and labelling of chemicals.

      • Understanding CLP
      • Understanding Seveso
      • Legislation
      • Classification of substances and mixtures
      • Labelling and packaging
      • Harmonised classification and labelling (CLH)
      • Alternative chemical name in mixtures
      • The role of testing in CLP

      C&L Inventory

      • What is the Classification and Labelling Inventory?
      • Notification to the C&L Inventory
      Addressing substances of concern
      EUCLEF EUCLEF
      • Poison centres website
      • Nanomaterials
      • Substitution to safer chemicals
      • Enforcement
    • BPR Biocidal Products Regulation

      BPR regulation aims to improve the functioning of the biocidal products market in the EU, while ensuring a high level of protection for humans and the environment.

      • Understanding BPR
      • Legislation
      • Upcoming deadlines
      • Active substances and suppliers

      approval of active substances

      • Approval
      • New active substance
      • Existing active substance
      • Biocidal Products Committee opinions on active substance approval
      • List of approved active substances

      Authorisation of biocidal products

      • National authorisation and mutual recognition
      • Union authorisation
      • Simplified authorisation
      • Product family

      Guidance and IT-tools

      • Guidance documents
      • Prepare a dossier - IUCLID
      • Submit a dossier - R4BP 3
      Appeals
      EUCLEF EUCLEF
    • PIC Prior Informed Consent Regulation

      The Prior Informed Consent Regulation administers the import and export of certain hazardous chemicals and places obligations on companies who wish to export these chemicals to non-EU countries.

      • Understanding PIC
      • Legislation
      • Export notification procedure
      • Explicit consent requirement

      lists of Chemicals subject to pic 

      • Chemicals subject to PIC
      • Export notifications
      • Import notifications
      • Explicit consent
       
      EUCLEF EUCLEF
    • CAD/CMD (OELs) Chemical Agents Directive and Carcinogens or Mutagens Directive

      Occupational exposure limit (OEL) values are derived within two legal frameworks that form an integral part of the EU’s mechanism for protecting the health of workers.

      CAD/CMD

      • Understanding CAD and CMD
      • Occupational exposure limits
      • Legislation
       
      EUCLEF EUCLEF
    • WFD Waste Framework Directive

      The Waste Framework Directive aims to protect the environment and human health from the generation and management of waste and to improve efficient use of resources.

       

      SCIP

      WFD

      • Understanding the Waste Framework Directive
      • SCIP
      • Suppliers of articles
      • Waste operators
      • Consumers and SCIP
      • SCIP support
      • Tools to prepare and submit SCIP notifications
      • Legislation
       
      EUCLEF EUCLEF
    • POPs Persistent Organic Pollutants Regulation

      The POPs Regulation bans or severely restricts the production and use of persistent organic pollutants in the European Union.

      • Understanding POPs
      • Proposals for new POPs
      • POPs legislation
      • Planning and reporting
      • Enforcement

      Substance lists

      • List of substances subject to the POPs Regulation
      • List of substances proposed as POPs
       
      EUCLEF EUCLEF
    • DWD Drinking Water Directive

       

      The revised Drinking Water Directive aims to protect citizens and the environment from the harmful effects of contaminated drinking water and to improve access to drinking water.

       

       

      DWD

      • Understanding DWD
      • European positive lists
      • Legislation
  • Consultations

    ECHA organises consultations to get feedback from all interested parties and to gather the widest possible range of scientific information for the regulatory processes

    REACH

    • Substances of very high concern identification
    • Draft recommendation for inclusion in the Authorisation List and consultation
    • Applications for authorisation
    • Submitted restrictions under consideration
    • Consultations on new scientific evidence
    • Current calls for comments and evidence
    • Current Testing Proposals

    CLP

    • Harmonised classification and labelling
    • Harmonised classification and labelling targeted consultations
    • Consultations on ECHA Executive Director’s requests

    BPR

    • Potential candidates for substitution
    • Derogations to the exclusion criteria

    CAD/CMD

    • Occupational exposure limits

    View all

  • Information on Chemicals

    This is unique source of information on the chemicals manufactured and imported in Europe. It covers their hazardous properties, classification and labelling, and information on how to use them safely.

    REACH

    • Registration statistics
    • Registered substances
    • EC Inventory
    • Dossier Evaluation status
    • PACT - Public Activities Coordination Tool
    • Substance Evaluation - CoRAP
    • Information on Candidate List substances in articles
    • Substances restricted under REACH
    • Authorisation List
    • Candidate List of substances of very high concern for Authorisation
    • Registry of restriction intentions until outcome
    • Registry of SVHC intentions until outcome

    CLP

    • C&L Inventory
    • Table of harmonised entries in Annex VI to CLP
    • Registry of CLH intentions until outcome

    Bpr

    • Biocidal Active Substances
    • Biocidal Products
    • List of active substances and suppliers

    PIC

    • Chemicals subject to PIC
    • Export notifications
    • Import notifications
    • Explicit consent
     
    EUCLEF EUCLEF

    POPS

    • List of substances subject to the POPs Regulation
    • List of substances proposed as POPs

    CAD/CMD

    • Occupational exposure limits - Activity list

    opinions and agreements

    • Restriction (RAC ad SEAC)
    • Authorisation of use of SVHC
      (RAC and SEAC)
    • SVHC identification (MSC)
    • Draft recommendation (MSC)
    • Draft CoRAP update (MSC)
    • Harmonised classification and labelling (RAC)
    • Active substance approval (BPC)
    • Union Authorisation (BPC)
    • OEL (RAC)
    • Executive Director request (RAC)
    • Executive Director request (SEAC)
    • Executive Director request (MSC)

    View all

  • Support

    The Support section provides tools and practical guidance to companies which have responsibilities under the EU chemicals legislation.

    REACH

    • Guidance on REACH
    • Identify your company obligations
    • Registration
    • Substance identification
    • Technical completeness check
    • Testing methods and alternatives
    • How to apply for authorisation
    • Restriction
    • How to submit downstream user reports
    • Socio-economic Analysis in REACH

    CLP

    • Guidance on CLP
    • Submission of CLH dossiers
    • Mixture classification

    BPR

    • Guidance on BPR
    • Emission scenario documents

    PIC

    • Guidance on PIC
    • Formats and templates

    •  
      Publications
       
    • Webinars
       
    • Small and medium enterprises
       
    • Getting started with EU chemicals legislation
       
    • The UK’s withdrawal from the EU
    EUCLEF EUCLEF
    Q&As
    Helpdesks
    Contact

    View all

Skip to Content
  1. ECHA
  2. Support
  3. Registration phases
  4. 4. What information you need
  5. How to avoid unnecessary testing on animals
  6. In vitro methods

Sign In

Return to Full Page
Select your profile:
Public authority or ECHA staff Personal or other account
  • If you are from a public authority or are a member of ECHA staff, select the public authority or ECHA staff profile to continue.
  • If you have an existing ECHA account (in REACH-IT, R4BP 3, ePIC or the Cloud Services), choose the personal or other account profile, and sign in with your credentials.
  • Not yet a user? Choose the personal or other account profile to sign up.

Route: .live2
  • Legislation
    • REACH
    • CLP
    • BPR
    • PIC
    • CAD/CMD (OELs)
    • WFD
    • POPs
    • DWD
  • Consultations
    • Previous consultations on ECHA’s Executive Director Requests to the Committees
    • Draft recommendation for inclusion in the Authorisation List and consultation
    • Applications for authorisation consultations
    • Consultations on new scientific evidence
    • Testing proposals consultation
    • Harmonised classification and labelling consultations
    • Submitted restrictions under consideration
    • ECHA Executive Director’s requests related to the CLH process
    • Current calls for comments and evidence
    • Consultation on potential candidates for substitution
    • Consultation on derogation to the exclusion criteria
    • ECHA's Executive Director Requests to the Committees
    • Harmonised classification and labelling targeted consultations
    • Consultation on a draft recommendation for amendment of Authorisation List entries
    • Consultations in the authorisation process
    • Substances of very high concern identification
    • Occupational exposure limits - Call for comments and evidence
    • Occupational exposure limits - Previous calls for comments and evidence
    • Occupational exposure limits – Consultations on OEL recommendation
    • Derogations for the protection of cultural heritage
    • Proposals for new POPs
  • Information on Chemicals
    • Registered substances
    • Registry of restriction intentions until outcome
    • Registry of SVHC intentions until outcome
    • Registry of CLH intentions until outcome
    • ECHA's current activities on restrictions
    • ECHA's completed activities on restriction
    • Annex III inventory
    • Pre-registered substances
    • EC Inventory
    • Dossier Evaluation status
    • PACT
    • Endocrine disruptor assessment list
    • PBT assessment list
    • Substance evaluation - CoRAP
    • RMOA list
    • Information on Candidate List substances in articles table
    • REACH registration statistics
    • C&L Inventory
    • Substances restricted under REACH
    • Biocidal Active Substances
    • Biocidal Products
    • List of active substances and suppliers
    • Chemicals subject to PIC
    • Transitional Measures
    • Information from the Existing Substances Regulation (ESR)
    • PBT/vPvB assessments under the previous EU chemicals legislation
    • Candidate List
    • Submitted recommendations
    • Adopted opinions and previous consultations on applications for authorisation
    • Authorisation List
    • Adopted opinions on restriction proposals
    • Mapping exercise – Plastic additives initiative
    • Occupational exposure limits substance evaluations
    • List of substances subject to POPs Regulation
    • List of substances proposed as POPs
    • EUCLEF
  • Support
    • Guidance
    • Getting started
    • Q&As Support
    • Testing methods and alternatives
    • Webinars
    • Dossier Submission Tools
    • National Helpdesks
    • Practical examples of exposure scenarios
    • Small and Medium-sized Enterprises (SMEs)
    • Registration phases
    • Practical examples of chemical safety reports
    • Substance identification
    • Authorisation
    • Restriction
    • Submission of CLH dossiers
    • Socio-economic analysis in REACH
    • QSAR Toolbox
    • Mixture classification
    • UK withdrawal from the EU
    • Recommendations to registrants
    • ECHA accounts and EU Login
    • Technical completeness check

European Chemicals Agency

Telakkakatu 6, P.O. Box 400, FI-00121 Helsinki, Finland
  • Sitemap
  • Legal Notice

Follow us

  • Facebook
  • LinkedIn
  • Twitter
  • YouTube

Welcome to the ECHA website. This site is not fully supported in Internet Explorer 7 (and earlier versions). Please upgrade your Internet Explorer to a newer version.

This website uses cookies to ensure you get the best experience on our websites.

Find out more on how we use cookies.