Navigation

  • Skip to Content

ECHA
Sign In

ECHA
  • About Us
    • Who we are
    • The way we work
    • Jobs
    • Procurement
  • Addressing Chemicals of Concern
  • Legislation
    • REACH
    • CLP
    • BPR
    • PIC
    • POPs
    • CAD/CMRD (OELs)
    • WFD
    • DWD
  • 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
    • Consultation on draft recommendation for inclusion in the Authorisation List
  • 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
  • Chemicals in our Life
    • What about animal testing?-TO-BE-DELETED
    • Use chemicals safely at work-TO-BE-DELETED
    • Which chemicals are of concern?-TO-BE-DELETED
    • Are there safer alternatives?-TO-BE-DELETED
    • How can I use chemicals safely?-TO-BE-DELETED
    • Why are chemicals important?-TO-BE-DELETED
    • Who is responsible for chemical safety?-TO-BE-DELETED
    • How European legislation on chemicals improves our lives
    • Why are nanomaterials important?-TO-BE-DELETED
  • Support
    • Getting started
    • Guidance
    • 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
    • Mixture classification
    • UK withdrawal from the EU
    • ECHA accounts and EU Login
    • Technical completeness check
    • Questions and answers
  • Addressing substances of concern
    • Universe of registered substances
    • Working with Groups
  • COVID-19 information
    • National information on covid-19
  • Contact
    • Regulatory support
    • Technical support
    • Additional support
  • migration
  • Jobs
  • EUCLEF
    • legislation-finder
    • legislation-profile-10-2011
    • legislation-profile-92-85
    • legislation-profile-98-24
    • legislation-profile-2017-164
    • legislation-profile-1223-2009
    • legislation-profile-540-2011
    • legislation-profile-2004-107
    • legislation-profile-2006-66
    • legislation-profile-94-62
    • legislation-profile-98-83
    • legislation-profile-2008-105
    • legislation-profile-2000-39
    • legislation-profile-2006-15
    • legislation-profile-2009-161
    • legislation-profile-91-322
    • legislation-profile-2004-37
    • legislation-profile-2007-42
    • legislation-profile-84-500
    • legislation-profile-94-33
    • legislation-profile-92-58
    • legislation-profile-2014-28
    • legislation-profile-648-2004
    • legislation-profile-91-271
    • legislation-profile-2011-65
    • legislation-profile-2016-2284
    • legislation-profile-2000-60
    • legislation-profile-2008-50
    • legislation-profile-2008-68
    • legislation-profile-2008-98
    • legislation-profile-2009-48
    • legislation-profile-2010-75
    • legislation-profile-2012-19
    • legislation-profile-2003-2003
    • legislation-profile-66-2010
    • legislation-profile-396-2005
  • SCIP Factsheet
  • ECHA Articles
  • Security incident on 07/12/2022

Sitemap

  • About Us
    • Who we are
      • Mission
      • Values
      • Organisation
        • Directors’ agenda
      • Executive Director
      • Directorates and Units
        • Registry of the Board of Appeal
        • Internal Audit Capability
      • Management Board
        • Management board meetings
      • Member State Committee
        • Meetings of the Member State Committee
          • 2023
      • Committee for Risk Assessment
        • Members of the RAC
      • Committee for Socio-Economic Analysis
        • Members of the SEAC
        • Meetings of the SEAC
      • Biocidal Products Committee
        • Working Groups
      • Enforcement Forum
        • Members of the Forum
          • Forum BPR Subgroup Members and Alternates
        • Meetings of the Forum
          • 2023
        • Forum's Open Sessions
        • Working groups
        • Forum enforcement projects
        • Enforceability of Restrictions
        • Training for enforcement trainers
        • Stakeholders
      • Board of Appeal
        • Who we are
        • Appeal procedure
        • Announcements
        • Hearings
        • Decisions
        • Contact
      • Staff statistics
    • The way we work
      • Plans and reports
        • Specific reports
        • Report archive
        • Annual Report 2021
      • Decisions of general application
      • ECHA Integrated Management System (IMS)
      • Procedures and Policies
        • Independence
        • Transparency
          • European Ombudsman
          • Complaints
          • Other jurisdictions
        • Code of good administrative behaviour
        • Access to documents
          • Factsheets
        • ECHA Procedures
      • Multilingual practice
        • Multilingual terminology database: IATE
      • Personal data protection
      • Financial management and budgetary reporting
      • Environmental management
    • Jobs
      • Open positions
      • Eligibility criteria
      • Staff
      • The recruitment process
      • What we offer
      • Work-life balance
      • Traineeships
      • Seconded National Experts
      • Inter-Agency Job Market
    • Procurement
      • Closed calls
  • Addressing Chemicals of Concern
  • Legislation
    • REACH
      • Understanding REACH
      • Substance Identification
      • Registration
        • Research and development (PPORD)
        • Data sharing
          • Inquiry
          • Joint submission
          • Data sharing disputes
        • Information requirements
          • Chemical safety report
            • Chemical safety report/Exposure scenario roadmap
              • Use maps
        • Publishing information from dossiers
      • Evaluation
        • Evaluation process
        • Actors
        • Dossier evaluation
          • Compliance checks
          • Examination of testing proposals
        • Substance Evaluation
          • Community rolling action plan
          • What happens after substance evaluation?
        • Progress in evaluation
          • Overall progress in evaluation
          • Progress in evaluation 2018
          • Progress in evaluation 2019
          • Progress in evaluation 2020
          • Progress in evaluation 2021
          • Progress in evaluation 2022
        • Recommendations to registrants
      • Authorisation
        • Authorisation process
        • Substances of very high concern identification
          • Candidate List obligations
        • Recommendation for the Authorisation List
        • Applications for authorisation
          • Downstream uses covered by granted authorisations
      • Restriction
        • Restriction procedure
          • Restriction process
        • ECHA’s activities on restrictions
        • Preparation of a restriction proposal
        • Consultations
        • Information on restricted substances
      • Communication in the supply chain
        • Extended safety data sheets
        • Manufacturers
        • Importers
        • Only representatives
        • Distributors
        • Downstream users
          • About downstream users
          • More on downstream user responsibilities
          • Other issues affecting downstream users
          • Formulators
        • Communication in the supply chain infographic
      • Candidate List substances in articles
        • Notification of substances in articles
        • Communication in the supply chain
      • Legislation
      • Alternatives to animal testing under REACH
      • Enforcement
        • National Inspectorates
      • Substitution to safer chemicals
        • Why substitute?
        • How to substitute?
        • Real-life cases
        • Funding and technical support
        • Find substitution partners
        • News and activities
        • Networks
        • Supply chain workshops
        • Data to prevent regrettable substitution
        • Online training on analysis of alternatives
      • Nanomaterials
        • Nanomaterials Expert Group
      • Assessment of regulatory needs
      • PBT assessment
      • Endocrine disruptor assessment
      • Cooperation with authorities and stakeholders
        • RIME+ Platform
        • PBT Expert Group
          • Management of PBT/vPvB substances under REACH
          • Supporting activities
          • List of PBT Expert Group members
        • Endocrine Disruptor Expert Group
          • List of Endocrine Disruptor Expert Group members
        • REACH Exposure Expert Group
        • PETCO Working Group
        • Plastic additives initiative
          • Comparing relative release potential
        • Metals and Inorganics Sectoral Approach
        • ECHA-CEFIC collaboration on dossier compliance
      • Addressing substances of concern
    • CLP
      • Understanding CLP
        • CLP Pictograms
          • CLP quiz
          • What does the label contain
      • Classification of substances and mixtures
      • Labelling and packaging
      • Harmonised classification and labelling (CLH)
      • Alternative chemical name in mixtures
      • Understanding Seveso
      • C&L Inventory
        • Notification to the C&L Inventory
      • Legislation
      • The role of testing in CLP
      • Enforcement
      • Substitution to safer chemicals
      • Nanomaterials
      • Addressing substances of concern
    • BPR
      • Understanding BPR
      • Upcoming deadlines
      • Approval of active substances
        • New active substance
        • Existing active substance
        • BPC opinions on active substance approval
        • List of approved active substances
        • BPC Opinions on Article 15(2)
      • Renewal of active substances
      • In situ generated active substances
      • Annex I amendment
        • Dossier submission
        • Evaluation process
        • Biocidal Products Committee opinions on inclusion in Annex I
      • Authorisation of biocidal products
        • National authorisation and mutual recognition
        • National authorisation and mutual recognition renewal
          • Dossier submission
          • National authorisation evaluation process
          • Mutual recognition evaluation process
          • BPC opinions on Article 38
        • Union authorisation
          • Dossier submission
          • Evaluation process
          • Opinions on union authorisation
        • Simplified authorisation
          • Application procedure
        • Product family
        • Same biocidal products authorisation
      • Technical equivalence
        • Application and assessment procedure
      • Active substances and suppliers
        • Application and assessment procedure
      • BPR Legislation
      • Product-types
      • Treated articles
      • Data sharing
        • Inquiry
      • Substitution to safer chemicals
      • Nanomaterials
      • BPR Coordination group
    • PIC
      • Understanding PIC
      • List of chemicals: Annex I
      • Export notification procedure
      • Explicit consent requirement
        • Proposing waivers through ePIC
      • PIC Legislation
      • Annual reporting on PIC exports and imports
      • PIC Circular
      • Reporting on information exchange
      • Reporting on the operation of PIC Regulation
    • POPs
      • Understanding POPs
      • Proposals for new POPs
      • Information on consultations
      • Legislation
      • Planning and reporting
      • Enforcement
    • CAD/CMRD (OELs)
      • Understanding CAD and CMRD
      • Occupational exposure limits
      • OEL Process
      • History to ECHA starting OEL work
      • Legislation
    • WFD
      • Understanding WFD
      • SCIP
        • Suppliers of articles
        • Waste operators
        • Consumers and SCIP
        • SCIP support
          • SCIP IT user group
          • Events
        • Tools to prepare and submit notifications
          • Candidate List Package
          • SCIP Format
          • Trial service
        • SCIP infographic
      • Legislation
    • DWD
      • Understanding DWD
      • European positive lists
      • Legislation
  • 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
      • Instructions for providing comments in applications for authorisation consultations
      • Statistics on received applications
      • Upcoming consultations on applications for authorisation
      • Applications for authorisation consultation windows
    • Submitted restrictions under consideration
    • Current calls for comments and evidence
    • Testing proposals consultation
      • Current Testing Proposals
        • temp-table
      • Previous Testing Proposals
    • 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 - Previous calls for comments and evidence
    • Occupational exposure limits – Consultations on OEL recommendation
      • Occupational exposure limits – Previous consultations on OEL recommendation
    • Derogations for the protection of cultural heritage
      • Previous consultations on derogations for the protection of cultural heritage
    • Proposals for new POPs
      • Previous consultations on proposals for new POPs
    • Other calls for comments and evidence
      • Other calls for comments and evidence - previous consultations
    • Consultation on draft recommendation for inclusion in the Authorisation List
  • 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
      • Removal of Pre-registrations
      • Substances of Interest
    • EC Inventory
    • Dossier Evaluation status
    • PACT
      • Understanding 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 requirements
      • Annex XV transitional reports
      • Voluntary risk assessment reports
    • Information from the Existing Substances Regulation (ESR)
    • PBT/vPvB assessments under the previous EU chemicals legislation
    • REACH registration statistics
      • Technical notes
    • 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
      • pregnant-women-protection
      • chemagts-oels-ann-1
      • chemagts-blvs-ann-2
      • chemagts-prohibitions-ann-3
      • chemagts-worker-protection-hazardous
      • indicative-oelvs-dir-2017-164
      • cosmetics-prohibited-subs
      • cosmetics-colorant
      • cosmetics-preservatives
      • cosmetics-uv-filters
      • cosmetics-restricted-subs
      • plastic-material-food-contact
      • plastic-subs-restricted-ann-2
      • ann-i-ii-dir-2004-107
      • batteries-accumulators-waste
      • lead-cadmium-migration-limits-ceramic
      • explosives-civil-uses
      • content-labelling-detergents
      • exempted-surfactants-phosphate
      • environmental-quality-standards
      • quality-criteria-water
      • indicative-oelvs-dir-91-322
      • indicative-oelvs-dir-2000-39
      • indicative-oelvs-dir-2006-15
      • indicative-oelvs-dir-2009-161
      • ann-approved-act-subs-plant-prot-prods
      • regen-cellulose-film-subs
      • workplace-signs
      • carcinogens-mutagens-oels
      • carcinogens-mutagens-dir-2004-37
      • young-people-at-work
      • heavy-metals-packaging-waste
      • air-ann-dir-2008-50
      • ambient-air-ozone-prec-subs-dir-2008-50
      • ann-x-priority-subs-water-dir-2000-60
      • dangerous-subs-eco-labels
      • fertilizer-list-ann-1-a-e-1
      • fertilizer-list-ann-1-e-2
      • fertilizer-list-ann-1-e-3
      • fertilizer-list-ann-1-f
      • integrated-pollution-prevention-control
      • ippc-ann-5-6-8-dir-2010-75
      • ippc-ann-7-organic-solvents-dir-2010-75
      • adr-dangerous-goods-lists-dir-2008-68
      • adn-dangerous-goods-lists-dir-2008-68
      • rin-dangerous-goods-lists-dir-2008-68
      • pesticides-mrls-ann-dir-396-2005
      • air-annual-emission-reporting-dir-2016-2284
      • restricted-subs-referred-art-4-rohs
      • exemptions-art-4-restrictions-rohs
      • allergenic-fragrances-banned-restricted-toys
      • substances-restricted-toys
      • urban-waste-water-treatment
      • hazardous-waste-properties-ann-3-dir-2008-98
      • directive-2012-19-weee-ann-7
      • EU-SAFETY_HEALTH_WORK-PREAMBLE
      • EU-WASTE_SHIPMENT-ANX_III_IIIA_IIIB_IV_V
      • EU-PESTICIDES_STATISTICS-ANX_III
      • EU-VOC_EMISSIONS-ART_3_1_4_1_6_1
      • EU-MARINE_ENVIRONMENTAL_POLICY-ART_3_8
      • EU-END_OF_LIFE_VEHICLES-ART_2_11
      • EU-END_OF_LIFE_VEHICLES-ANX_II_SPECIFIC_EXEMPTIONS
      • EU-END_OF_LIFE_VEHICLES-ANX_II_GENERAL_EXEMPTIONS
      • EU-ACTIVE_INTELLIGENT_FCM-ART_5_2_c_i
      • EU-FOOD_CONTACT_MATERIALS-ANX_I
      • EU-AEROSOL_DISPENSERS-ANX_1_8_1_9_2_2
      • EU-CONSTRUCTION_PROD-ART_6_5
      • EU-CONSTRUCTION_PROD-ANX_I_3
      • EU-IMPLANTABLE_MEDICAL_DEVICES-ART_3_ANX_1
      • EU-IN_VITRO_MEDICAL_DEVICES-ART_3_ANX_1
      • EU-MEDICAL_DEVICES-ANX_I_7_8
      • EU-PRESSURE_EQUIPMENT-ART_13_1_a
      • EU-PRODUCT_SAFETY-ART_2
      • EU-PLANT_PROTECTION-ANX_III
      • EU-MEDICAL_DEVICES_REGULATION-ANX_I_SEC_10
      • EU-IOELV_LIST_5-ANX_I
      • EU-FERTILISING_PRODUCTS-ANX_I_PART_I
      • EU-FERTILISING_PRODUCTS-ANX_I_PART_II
      • EU-FERTILISING_PRODUCTS-ANX_II_PART_I
      • EU-FERTILISING_PRODUCTS-ANX_III_PART_II
      • EU-IN_VITRO_MEDICAL_DEVICE_REG-ART_5_2_ANX_1
      • EU-WORKER_CARC_MUTA-ANX_IIIa
    • Previous consultation of draft recommendatons for inclusion in the authorisation list
  • Chemicals in our Life
    • What about animal testing?-TO-BE-DELETED
    • Use chemicals safely at work-TO-BE-DELETED
    • Which chemicals are of concern?-TO-BE-DELETED
    • Are there safer alternatives?-TO-BE-DELETED
    • How can I use chemicals safely?-TO-BE-DELETED
    • Why are chemicals important?-TO-BE-DELETED
    • Who is responsible for chemical safety?-TO-BE-DELETED
    • How European legislation on chemicals improves our lives
    • Why are nanomaterials important?-TO-BE-DELETED
      • Making tiny stuff do big things-TO-BE-DELETED
      • Do you work with nanomaterials?-TO-BE-DELETED
      • Nanomaterials and health-TO-BE-DELETED
      • Fighting cancer using nanotechnology-TO-BE-DELETED
  • Support
    • Getting started
      • Manufacturer
      • Importer
      • Only representative
      • Distributor
      • User of chemicals
      • Biocides supplier or user
      • Trader in very hazardous chemicals
      • Exemptions?
      • Finding help
      • REACH, CLP and biocides for non-EU companies
        • Enquiry on biocides
    • Guidance
      • Consultation Procedure
      • Guidance Documents
      • Guidance in a Nutshell
      • Practical Guides
      • Formats and templates
    • Testing methods and alternatives
      • OECD and EU test guidelines
    • Webinars
    • Dossier Submission Tools
      • Manuals
      • REACH-IT
        • Registration Process
        • PPORD
        • Notifying substances in articles
        • Submitting downstream user notification of authorised uses
        • Submitting a downstream user report for unsupported uses
        • Submitting a downstream user report for classification differences
        • How to submit and update your C&L notification
        • Requesting an alternative chemical name in mixtures
      • IUCLID
      • CHESAR
      • SPC Editor
      • R4BP 3
        • Biocides Submission Manuals
        • Supporting documents
        • Active substances
        • National authorisations
        • Technical equivalence
        • Union authorisations
        • Simplified authorisations
      • ePIC
        • ePic manuals
      • ECHA Cloud Services
        • Q&As
      • Interact Portal
      • EUSES
      • System-to-system submission service
    • National Helpdesks
    • Practical examples of exposure scenarios
    • Practical examples of chemical safety reports
    • Small and Medium-sized Enterprises (SMEs)
      • SME fees under REACH and CLP
        • How to determine the company size category
        • What to do if you incorrectly indicated the SME size category
        • SME verification
        • Administrative charges
      • SME fees under BPR
    • Recommendations to registrants
      • General recommendations
      • Registration
      • Substance identification
      • Standard information requirements
      • Adaptations
      • Exposure assessment and risk characterisation
      • Classification and labelling
      • Dossier evaluation decisions
      • Substance evaluation decisions
    • Registration phases
      • 1. Your registration obligations
        • Do I need to register?
        • Does my substance need to be registered?
        • Do I reach the one tonne a year threshold?
        • How to characterise and identify your substance
        • What you need to consider for your business
        • What you need to submit
      • 2. Finding your co-registrants
        • Establishing substance sameness
      • 3. Get organised with your co-registrants
        • Creating a new joint submission
        • Joining an existing joint submission
          • Dos and Don'ts for data sharing negotiations
        • Practical advice for sharing data
      • 4. Assessing hazard and risk
        • Information requirements: 1 to 10 tonnes per year
          • Reduced information requirements
        • Information requirements: 10 to 100 tonnes per year
        • Information requirements: 100 to 1000 tonnes per year
        • Information requirements: 1000 tonnes or above per year
        • Adaptations to the standard information requirements
        • How to avoid unnecessary testing on animals
          • Weight of evidence
          • QSAR models
          • In vitro methods
          • Grouping of substances and read-across
        • Strategy for gathering your data
          • Practical considerations before testing
          • Collecting information on uses
      • 5. Creating your registration dossier
        • What is IUCLID?
        • How to create your registration dossier with IUCLID cloud
        • How to create your registration dossier with IUCLID
        • How to create your registration dossier in REACH-IT
      • 6. Submitting your registration dossier
        • From submission to decision
      • 7. Keeping your dossier up to date
        • Respect the deadlines for updating
        • Monitor the triggers for updating
        • Collaborate with your co-registrants
        • Prepare for updating your registration
        • Update and submit your registration
        • How to update your previously notified substance (NONS)
        • How to make changes to joint submissions
    • Substance identification
      • Why is it important to get it right?
      • What is a substance?
      • What is not a substance?
      • How to characterise and identify your substance
      • Four steps to successful substance identification
      • Sector-specific support for substance identification
        • Oleochemicals
        • Essential oils
        • Petroleum products
        • Hydrocarbon solvents
        • Complex inorganic pigments
        • Metals
      • How to change your substance identifier
    • Restriction
      • Information for authorities and stakeholders
    • Authorisation
      • Substances of very high concern identification
      • How to apply for authorisation
        • Are you affected by authorisation?
        • Develop an application strategy
          • Submission windows
          • Partners service for applicants
          • Simplified applications for authorisation for legacy spare parts
        • Start preparing your application
          • Formats for applications for authorisation
          • Evaluating applications
          • Previous events on appliction for authorisation
          • Information on applying for authorisation by Member States and industry organisations
        • Notify ECHA and request a teleconference based information session
          • Teleconference Based Information Sessions
          • Teleconference based information sessions - terms and conditions of use
        • Finalise your application
        • Submit your application
        • Engage during the opinion development
        • Fulfil your obligations
        • Submit a review report if you still need to use the substance
        • Ask ECHA about authorisation applications
    • Socio-economic analysis in REACH
      • SEA web portal
      • Willingness to pay to avoid certain health impacts
      • Network of REACH SEA and Analysis of Alternatives practitioners
      • Health utility metrics in chemicals impact assessment
    • Submission of CLH dossiers
    • Mixture classification
      • Where do I start?
      • Identify all available information
      • Examine available information
      • Evaluate information against classification criteria
      • Decide on classification and labelling
      • Review the classification
    • UK withdrawal from the EU
      • Know your role
        • UK-company based in Northern Ireland
        • Former UK-based REACH registrant
        • UK-based manufacturer or supplier under the BPR
        • EU-based company
        • UK-based mixture supplier
        • UK-based authorisation holder under REACH
        • EU downstream user of an authorised substance
      • Advice to companies
        • Q&As
      • Procurement and contracts
    • ECHA accounts and EU Login
    • Technical completeness check
      • Validation assistant
        • How to submit an enquiry about the Validation assistant
      • Manual verification
        • Substance identification
        • Data-waiving justifications
          • Specific advice
        • Testing proposals on vertebrate animals
        • Justification for opting-out
        • Chemical safety report and uses
        • Specific requirements for nanoforms
      • Failures and rejections
    • Questions and answers
  • Addressing substances of concern
    • Universe of registered substances
      • How does the chemical universe mapping work?
    • Working with Groups
  • COVID-19 information
    • National information on covid-19
  • Contact
    • Regulatory support
    • Technical support
    • Additional support
  • migration
  • Jobs
  • EUCLEF
    • legislation-finder
    • legislation-profile-10-2011
    • legislation-profile-92-85
    • legislation-profile-98-24
    • legislation-profile-2017-164
    • legislation-profile-1223-2009
    • legislation-profile-540-2011
    • legislation-profile-2004-107
    • legislation-profile-2006-66
    • legislation-profile-94-62
    • legislation-profile-98-83
    • legislation-profile-2008-105
    • legislation-profile-2000-39
    • legislation-profile-2006-15
    • legislation-profile-2009-161
    • legislation-profile-91-322
    • legislation-profile-2004-37
    • legislation-profile-2007-42
    • legislation-profile-84-500
    • legislation-profile-94-33
    • legislation-profile-92-58
    • legislation-profile-2014-28
    • legislation-profile-648-2004
    • legislation-profile-91-271
    • legislation-profile-2011-65
    • legislation-profile-2016-2284
    • legislation-profile-2000-60
    • legislation-profile-2008-50
    • legislation-profile-2008-68
    • legislation-profile-2008-98
    • legislation-profile-2009-48
    • legislation-profile-2010-75
    • legislation-profile-2012-19
    • legislation-profile-2003-2003
    • legislation-profile-66-2010
    • legislation-profile-396-2005
  • SCIP Factsheet
  • ECHA Articles
  • Security incident on 07/12/2022

EU Privacy Disclaimer

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

Read More
Powered By Liferay

internet-explorer-outdated-warning

the-echa-website-uses-cookies

find-out-more-on how-we-use-cookies