Information for authorities and stakeholders
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Documents et informations d'appui
- Introduction
- Guides
- Méthodes d'essai et alternatives
- Webinaires
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Outils pour la soumission des données
- Manuals
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REACH-IT
- Processus d'enregistrement
- RDAPP
- Notification de substances contenues dans des articles
- Soumettre une notification d'utilisateur en aval concernant des utilisations autorisées
- Soumettre un rapport d'utilisateur en aval concernant des utilisations non couvertes
- Soumettre un rapport d'utilisateur en aval concernant des différences de classification
- Comment présenter et mettre à jour votre notification C&L
- Demande d'un nom chimique de remplacement pour les substances contenues dans des mélanges
- IUCLID
- CHESAR
- SPC
- R4BP 3
- ePIC
- Services en nuage de l'ECHA
- Interact Portal
- EUSES
- System-to-system submission service
- Services d’assistance nationaux
- Exemples pratiques de scénarios d'exposition
- Exemples pratiques de rapports sur la sécurité chimique
- Petites et moyennes entreprises (PME)
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Recommandations aux déclarants
- Recommandations générales
- Enregistrement
- Identification des substances
- Exigences en matière d’informations standard
- Adaptations
- Évaluation de l’exposition et caractérisation des risques
- Classification et étiquetage
- Décision dans le cadre de l’évaluation d’un dossier
- Décision dans le cadre de l’évaluation d’une substance
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Phases d’enregistrement
- 1. Vos obligations d'enregistrement
- 2. Trouver vos codéclarants
- 3. Organisez-vous avec vos co-déclarants
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4. Évaluation des dangers et des risques
- Exigences en matière d'information: 1 à 10 tonnes par an
- Exigences en matière d'information: 10 à 100 tonnes par an
- Exigences en matière d’information: 100 à 1000 tonnes par an
- Exigences en matière d’information: 1000 tonnes ou plus par an
- Adaptations aux exigences en matière d'informations standard
- Comment éviter les essais inutiles sur les animaux
- Stratégie de collecte des données
- 5. Créez votre dossier d’enregistrement
- 6. Soumettez votre dossier d’enregistrement
- 7. Comment s’organiser pour les mises à jour de dossier
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Identification de la substance
- Pourquoi est-il important de ne pas se tromper?
- Qu'est-ce qu'une substance?
- Qu'est-ce qui n'est pas une substance?
- Comment caractériser et identifier votre substance
- Quatre étapes vers l'identification réussie d'une substance
- Assistance spécifique au secteur pour l'identification des substances
- Comment modifier l'identifiant de votre substance
- Restriction
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Autorisation
- Identification des susbtances extrêmement préoccupantes
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Comment présenter une demande d’autorisation
- L'autorisation vous concerne-t-elle?
- Élaborez une stratégie pour déposer une demande
- Débutez la préparation de votre demande
- Notifiez l'ECHA et demandez une séance d'information préalable à la soumission
- Finalisez votre demande
- Soumettez votre demande
- Participez à l'élaboration de l'avis
- Respectez vos obligations
- Soumettez un rapport d’examen si vous avez toujours besoin d’utiliser la substance
- Interrogez l'ECHA sur les demandes d'autorisation
- Analyse socio-économique dans REACH
- Soumission de dossiers CLH
- Classification des mélanges
- Le retrait du Royaume-Uni de l’UE
- ECHA accounts and EU Login
- Contrôle du caractère complet (aspect technique)
- Questions and answers
- ECHA CHEM
Information for authorities and stakeholders
Restrictions under consideration and other activities on restrictions
You may wish to regularly check whether a substance you are interested in is currently undergoing a restriction proposal or to a review the work ECHA is conducting in relation to restrictions.
If you sign up to receive ECHA's e-News, you will receive an alert once the Registry of Intentions is updated, a consultation starts or there is a relevant call for comments and evidence.
You can also provide comments and information during the consultation using the specific webform available on ECHA's consultation website. The consultation is the only official channel to deliver comments including additional information to be taken into account by the Committees for Risk Assessment (RAC) and Socio-economic Analysis (SEAC) during the opinion-making process.
For the substance for which a restriction is proposed, the start of the consultation is informed by ECHA to:
- the registrants of the substance
- notifiers to the Classification and Labelling Inventory of the substance
- registrants of alternatives identified in the restriction dossier
- notifiers to the Classification and Labelling Inventory of the alternatives, and
- any other relevant stakeholders.
Member States will also receive a communication from ECHA shortly after the start of the consultation with the relevant links. ECHA welcomes any initiative by Members States to promote the participation in the consultation at a national level, involving relevant stakeholders from industry, local authorities and experts from the academic sector, NGOs and individual citizens.
The comments and information submitted will be taken into account by the Committees for Risk Assessment (RAC) and Socio-economic Assessment (SEAC) during the opinion-making process. A specific form is available on ECHA's website to submit comments during the legal timeframe. Comments received after the legal deadline will not be considered by the Committees.
ECHA may also hold consultations such as "calls for comments and evidence" during the preparation of a restriction dossier, review report or a guideline. All interested parties, including producers or consumers of alternative substances or technologies are welcome to contribute.
The information for dossier submitters may also give you additional information on how the restriction proposals are processed.
Existing restrictions
Authorities as well as industry, consumers and other stakeholders, such as NGOs, academic experts, etc. that are interested in existing restrictions can look at the restriction entries from Annex XVII to REACH.
Further information is provided in the Q&As on ECHA's website.
The table under 'Substances restricted under REACH' provides all restrictions and Q&As including relevant links to standards.
If you have questions on restriction entries, your national helpdesk is the first point of contact and can provide a wide range of information. If you are a stakeholder from outside the EU, please contact the ECHA Helpdesk.
Enforcement of restrictions is the responsibility of each Member State. This means that the verification of the compliance of the duty holders with restriction provisions under REACH is carried out by the national enforcement authorities. ECHA hosts the Forum for Exchange of Information on Enforcement and coordinates a network of Member State authorities responsible for enforcement.
- Inputting to the consultation phase of the Annex XV restriction report and SEAC draft opinion [PDF][EN]
- Guidance for the preparation of an Annex XV dossier for restrictions [PDF][EN]
- Guidance for Socio-economic analysis – Restrictions [PDF][EN]
- Addendum: Calculation of compliance costs [PDF][EN]
- Fact sheet Socio-economic analysis – Restrictions [PDF][EN]
- Guidance for downstream users [PDF][EN]
- Requirements for substances in articles [PDF][EN]