EU Privacy Disclaimer

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

Read More
An agency of the European Union European Union Flag
  • Sign In
  • Quick Tools
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
    • 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
    • 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
      • SCIP Database
      • Suppliers of articles
      • Waste operators
      • Consumers and SCIP
      • SCIP support
      • Tools to prepare and submit SCIP notifications
      • Legislation
       
      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
    • 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

    • Consultations - Occupational Exposure Limits
    • Calls for evidence - 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

    WFD

    • SCIP Database
    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

Navigation

  • Skip to Content
  1. ECHA
  2. Support
  3. Authorisation
  4. How to apply for authorisation
  5. Previous events on appliction for authorisation

Previous events on appliction for authorisation

  • How to apply for authorisation
    • Are you affected by authorisation?
    • Develop an application strategy
    • Start preparing your application
    • Teleconference Based Information Sessions
    • Teleconference based information sessions - terms and conditions of use
    • Submission windows
      • Previous submission windows
    • Notify ECHA and request a teleconference based information session
    • Finalise your application
    • Formats for applications for authorisation
    • Submit your application
    • Engage during the opinion development
    • Fulfil your obligations
    • Evaluating applications
    • Previous events on appliction for authorisation
    • Partners service for applicants
    • Information on applying for authorisation by Member States and industry organisations
    • Ask ECHA about authorisation applications
    • Submit a review report if you still need to use the substance
    • Simplified applications for authorisation for legacy spare parts

Previous events on appliction for authorisation

  • 29-30 April 2014 ECHA workshop on sharing experience on applications for authorisation
  • 28-29 April 2014 ECHA seminar on Applications for Authorisation
  • 27-28 March 2014 ECHA Workshop on submitting applications for authorisation for chromates in an efficient way
  • 2 December 2013 Space Stakeholders' Day on REACH
  • 17 June 2013 ECHA information session on Critical Raw Materials and REACH
  • 17 June 2013 Seminar on Applications for Authorisation
  • 11-12 February 2013 Seminar on applications for authorisation
  • 23 January 2013 EASA/ECHA workshop on airworthiness and REACH authorisation
  • 1-2 October 2012 Seminar on applications for authorisation
  • 2-3 October 2012 Workshop on analysing alternatives and socio-economic impacts in authorisation applications
  • 28 November 2011 Seminar on the publication of information from the applications for authorisation process with industry representatives
  • 7 July 2011 Seminar on applications for authorisation with NGOs and trade unions
  • 12 April 2011 Seminar on applications for authorisation with industry

EU Privacy Disclaimer

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

Read More
  • About Us
    • Who we are
    • The way we work
    • Jobs
    • Procurement
  • Consultations
    • Consultations in the authorisation process
    • Substances of very high concern identification
    • Consultation on draft recommendation for inclusion in the Authorisation List
    • Applications for authorisation consultations
    • Submitted restrictions under consideration
    • Current calls for comments and evidence
    • Testing proposals consultation
    • Harmonised classification and labelling consultations
    • Harmonised classification and labelling targeted consultations
    • ECHA Executive Director’s requests related to the CLH process
    • Consultation on potential candidates for substitution
    • Consultation on derogation to the exclusion criteria
    • Previous consultations on ECHA’s Executive Director Requests to the Committees
    • ECHA's Executive Director Requests to the Committees
    • Consultation on a draft recommendation for amendment of Authorisation List entries
    • Occupational exposure limits - Call for comments and evidence
    • Occupational exposure limits – Consultations on OEL recommendation
    • Derogations for the protection of cultural heritage
    • Proposals for new POPs
    • Other calls for comments and evidence
  • Information on Chemicals
    • Registry of CLH intentions until outcome
    • Registry of restriction intentions until outcome
    • Registry of SVHC intentions until outcome
    • Registered substances
    • Annex III inventory
    • Pre-registered substances
    • EC Inventory
    • Dossier Evaluation status
    • PACT
    • Assessment of regulatory needs list
    • PBT assessment list
    • Endocrine disruptor assessment list
    • Substance evaluation - CoRAP
    • Information on Candidate List substances in articles table
    • 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
    • REACH registration statistics
    • Candidate List
    • Adopted opinions and previous consultations on applications for authorisation
    • Authorisation List
    • Adopted opinions on restriction proposals
    • ECHA's current activities on restrictions
    • ECHA's completed activities on restriction
    • Mapping exercise – Plastic additives initiative
    • Occupational exposure limits substance evaluations
    • List of substances subject to POPs Regulation
    • List of substances proposed as POPs
    • EUCLEF
    • Previous consultation of draft recommendatons for inclusion in the authorisation list
  • Support
    • Getting started
    • Guidance
    • Q&As Support
    • Testing methods and alternatives
    • Webinars
    • Dossier Submission Tools
    • National Helpdesks
    • Practical examples of exposure scenarios
    • Practical examples of chemical safety reports
    • Small and Medium-sized Enterprises (SMEs)
    • Recommendations to registrants
    • Registration phases
    • Substance identification
    • Restriction
    • Authorisation
    • Socio-economic analysis in REACH
    • Submission of CLH dossiers
    • How to improve your dossier
    • QSAR Toolbox
    • Mixture classification
    • UK withdrawal from the EU
    • ECHA accounts and EU Login
    • Technical completeness check
  • Contact
    • Regulatory support
    • Technical support
    • Additional support
  • Jobs

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.