Комитет за оценка на риска
The Committee for Risk Assessment (RAC) prepares the opinions of ECHA related to the risks of substances to human health and the environment in the following REACH and CLP processes. The final decisions are taken by the European Commission through a regulatory committee procedure.
Harmonised Classification and Labelling
RAC examines the proposals for harmonised classification and labelling and gives an opinion on the proposed harmonised classification of substances as carcinogenic, mutagenic, toxic for reproduction or as a respiratory sensitiser, as well as other effects on a case-by-case basis.
Restriction
The Committee evaluates whether the proposed restriction on manufacture, placing on the market or use of a substance is appropriate in reducing the risk to human health and the environment. This includes the assessment of comments submitted by third parties.
Authorisation
RAC assesses the risk of a substance arising from the uses of a substance when an application for authorisation is submitted. This includes an assessment of the appropriateness and effectiveness of the risk management measures as described in the authorisation application, and if relevant, of the risks of possible alternatives. Third party contributions linked to the application will also be assessed.
ECHA's Executive Director's requests
RAC gives an opinion on request from the Executive Director of ECHA relating to risks to human health and the environment on any other aspects concerning the safety of substances on their own, in preparations or in articles.
The Committee also provides scientific support to improve the cooperation between the Community, its Member States, international organisations and third countries relating to the safety of substances, as well as active participation in technical assistance and capacity building activities on the sound management of chemicals in developing countries.
Meetings
Meeting dates 2012 (tentative)
- 06-09 March
- 12-15 June
- 10-14 September
- 26-30 November
As specified by the RAC rules of procedure, the meetings of the Committee may be open to advisers, invited experts and observers at the request of the Committee members or ECHA's Management Board.
Composition
The members of RAC are appointed by ECHA's Management Board based on candidates nominated by the Members States for a renewable term of three years.
List of nominees for the Committee for Risk Assessment [PDF]
- CV [PDF]
- Declaration of interests [PDF]
Related links
- Meetings (agendas and minutes)
- List of RAC members with their CVs and Declarations of interest
- Harmonised Classification and Labelling
- RAC opinions on proposals for harmonised classification and labelling
- Restrictions
- RAC opinions on restrictions under consideration
- Applications for Authorisation
- Opinions adopted under specific ECHA's Executive Director requests
Related documents
- RAC Working Procedure on accordance check of a CLH dossier [PDF]
- RAC Working Procedure for processing of a CLH dossier [PDF]
- RAC working procedure on the conformity check of Annex XV restriction dossiers [PDF]
- RAC working procedure on processing of Annex XV restriction dossiers [PDF]
- Rules of procedure of RAC [PDF]
- List of the agreed RAC STO observers [PDF]
- The procedure for admission of STO observers [PDF]