Registry of restriction intentions until outcome

Registry of restriction intentions until outcome

Registry of restriction intentions until outcome

The registry of restriction intentions until outcome lists the intentions and Annex XV restriction proposals received by ECHA.

A restriction proposal may be prepared by a Member State or by ECHA at the request of the Commission or on its own initiative for substances in the Authorisation List. It is a legal requirement for a Member State to notify ECHA of its intention to prepare a restriction dossier. The advance notice enables interested parties to plan and prepare for commenting later on.

Interested parties can follow the progress of a proposal through the restriction process, from the notification of the intention to the adoption of the final opinions by the Committee for Risk Assessment (RAC) and the Committee for Socio-economic Analysis (SEAC), and the adoption of the restriction by the European Commission.

Stakeholders are encouraged to submit any relevant information to the dossier submitters during the preparation of the restriction proposal and during the consultations. Information to motivate any exemptions to the scope described in the intention is particularly useful to receive in the preparatory phase of the dossier.

1,6,7,8,9,14,15,16,17,17,18,18-Dodecachloropentacyclo[12.2.1.16,9.02,13.05,10]octadeca-7,15-diene (“Dechlorane Plus”™)

covering any of its individual anti- and syn-isomers or any combination thereof EC / List no: - CAS no: -
CLP Annex VI Index number
Further substance information
Non-exhaustive list of relevant numerical identifiers for the Candidate List entry “1,6,7,8,9,14,15,16,17,17,18,18-Dodecachloropentacyclo[12.2.1.16,9.02,13.05,10]octadeca-7,15-diene (“Dechlorane Plus”TM) [covering any of its individual antiand syn- isomers or any combination thereof]”, see: https://echa.europa.eu/documents/10162/9aa77dde-f0fc-4422-2c00-55b620e57552
Submitter(s)
Norway
Details on the scope of restriction
The proposal intends to restrict the manufacture, use and placing on the market of Dechlorane Plus™ as substances, constituents of other substances, mixtures and articles.
Reason for restriction
Dechlorane Plus is a substance of very high concern due to its very persistent and very bioaccumulating properties. The substance is widely detected in the global environment and some studies indicate increasing concentrations. Dechlorane plus has also been detected in human blood, placenta and breast milk. Norway has submitted a proposal to list Dechlorane Plus and its syn- and anti-isomers in Annexes A, B and/or C to the Stockholm Convention on Persistent Organic Pollutants.
Remarks
Status
Opinions adopted
Date of intention
26-Aug-2020
Expected date of submission
09-Apr-2021
Withdrawal date
Reason for withdrawal
Start of Call for Evidence consultation
01-Apr-2020
Deadline for comments on the Call for Evidence
15-Jun-2020
Start of second Call for Evidence consultation
Deadline for comments on the second Call for Evidence
Start of third Call for Evidence consultation
Deadline for comments on the third Call for Evidence
Restriction report (and annexes)
Information note on restriction report
Start of Annex XV report consultation
23-Jun-2021
1st deadline for comments on Annex XV report
28-Jul-2021
Final deadline for comments on Annex XV report
03-Jan-2022
Comments on Annex XV report
Opinion of RAC (and minority positions) and Forum Enforceability Advice (as of September 2023)
Draft opinion of SEAC
RAC & SEAC (draft) Background document (and annexes)
Start of SEAC draft opinion consultation
17-Mar-2022
Deadline for comments on SEAC draft opinion
16-May-2022
Comments on SEAC draft opinion
Compiled RAC and SEAC opinion (and minority positions)
Final background document (and annexes)
Adopted restriction/Commission communication
Latest update
12-Sep-2022
First published
02-Sep-2020

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