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6/25/2021 legislation-profile - ECHA

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LEGISLATION CONSULTATIONS INFORMATION ON CHEMICALS SUPPORT

ECHA > EUCLEF > CMD - Carcinogens and Mutagens Directive

CMD - Carcinogens and Mutagens Directive


Directive 2004/37/EC of the European Parliament and of the Council of 29 April 2004 on the protection of workers from the risks related to exposure to
carcinogens or mutagens at work (Sixth individual Directive within the meaning of Article 16(1) of Council Directive 89/391/EEC)

Scope
SUBSTANCE LISTS
Exemptions Scope
CMD - Carcinogens and
Regulatory activities Mutagens Directive, Annex III
This Directive has its aim the protection of workers against risks to
Relevant product types their health and safety, including the prevention of such risks, arising - OELVs
or likely to arise from exposure to carcinogens or mutagens at work.It Carc and Muta Directive,
Reference documents
lays down particular minimum requirements in this area, including limit Annex I - Substances,
Obligations based on CLP hazard values. (Art. 1 (1)) This Directive shall apply to activities in which Mixtures & Processes
class workers are or are likely to be exposed to carcinogens or mutagens as
a result of their work. (Art. 3(1)) SEE ALSO
Obligations based on properties of
concerns

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EU-level occupational exposure Exemptions Chemical, Physical and


limits Biological Agents at Work
The Directive shall not apply to workers expose only to radiation Directive
EU-level emission limit values
covered by the Treaty establishing the European Atomic Energy OELs - Occupational Exposure
Substance-centric data source(s) Community. (Art.1 (2)) As regards asbestos, which is dealt with by Limits - 1st list
at the EU level
Directive 83/477/EEC, the provisions of this Directive shall apply
OELs - Occupational Exposure
Industry submission system in whenever they are more favourable to health and safety at work. (Art.
Limits - 2nd list
place 1(4))
OELs - Occupational Exposure
Format for industry submission
Limits - 3rd list
Owner OELs - Occupational Exposure
Regulatory activities Limits - 4th list
Update process

Amendments
(a) Risk assessment by employer (Art. 3) (b) Submission of information
for the competent authorities by employer - where the results of the See a problem or have
assessment referred to in Article 3(2) reveal a risk to workers' health or feedback?
View Legislation Summary
safety, employers, shall, when requested, make available to the
View Full Legislation competent authority. (Art. 6) (c) MS Health surveillance - the MS shall
establish, in accordance with their national laws and/or practice,
arrangements for carrying out relevant health surveillance of workers.
(Art. 14)

Relevant product types


No reference data required

Reference documents
Yes Directive 89/391/EC Regulation (EC) No 1272/2008

Obligations based on CLP hazard class


Yes. Definition of 'limit value', 'carcinogen' and 'mutagen'. Reference is
made to Regulation (EC) No 1272/2008.

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Obligations based on properties of concerns


Yes Article 3- Determination and assessment of risks

EU-level occupational exposure limits


Yes Annex III of the Directive

EU-level emission limit values


No provision

Substance-centric data source(s) at the EU level


Not in place

Industry submission system in place


Not in place

Format for industry submission


Not specified

Owner
European Agency for Health and Safety at Work (OSHA)

Update process
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According to Article 16 of the Directive, the Council shall, in accordance


with the procedure laid down in Article 137 (2) of the Treaty, set out
limit values in Directives on the basis of available information. Annexes
I and III may be amended in accordance only with the procedure laid
down in Article 137 (2) of the Treaty. (Art. 17 (1)) Purely technical
adjustments to Annex II in the light of technical progress, changes in
international regulations or specifications and new findings in the field
of carcinogens or mutagens shall be adopted in accordance with the
procedure laid down in Article 17 of the Directive 89/391/EC.

Amendments
Corrigendum to Directive 2004/37/EC of 29 April 2004 on the
protection of workers from the risks related to exposure to carcinogens
or mutagens at work (Sixth individual Directive within the meaning of
Article 16(1) of Council Directive 89/391/EEC) (codified version)
DIRECTIVE 2014/27/EU OF THE EUROPEAN PARLIAMENT AND OF THE
COUNCIL of 26 February 2014 DIRECTIVE (EU) 2017/2398 OF THE
EUROPEAN PARLIAMENT AND OF THE COUNCIL of 12 December 2017
DIRECTIVE (EU) 2019/130 OF THE EUROPEAN PARLIAMENT AND OF
THE COUNCIL of 16 January 2019 DIRECTIVE (EU) 2019/983 OF THE
EUROPEAN PARLIAMENT AND OF THE COUNCIL of 5 June 2019
REGULATION (EU) 2019/1243 OF THE EUROPEAN PARLIAMENT AND OF
THE COUNCIL of 20 June 2019

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LEGISLATION CONSULTATIONS INFORMATION ON CHEMICALS SUPPORT

REACH Previous consultations on ECHA’s Registered substances Guidance


Executive Director Requests to the
CLP Committees Registry of restriction intentions until Getting started
outcome
BPR Draft recommendation for inclusion in Q&As Support
the Authorisation List and consultation Registry of SVHC intentions until
PIC outcome Testing methods and alternatives

CAD/CMD (OELs) Applications for authorisation Webinars


consultations Registry of CLH intentions until
WFD outcome Dossier Submission Tools
Consultations on new scientific
POPs evidence ECHA's current activities on National Helpdesks
restrictions
DWD Testing proposals consultation Practical examples of exposure
ECHA's completed activities on scenarios
Harmonised classification and labelling restriction
consultations Small and Medium-sized Enterprises
Annex III inventory (SMEs)
Submitted restrictions under
consideration Pre-registered substances Registration phases

ECHA Executive Director’s requests EC Inventory Practical examples of chemical safety


related to the CLH process Dossier Evaluation status reports

Current calls for comments and PACT Substance identification


evidence
Endocrine disruptor assessment list Authorisation
Consultation on potential candidates
for substitution PBT assessment list Restriction

Consultation on derogation to the Substance evaluation - CoRAP Submission of CLH dossiers


exclusion criteria Socio-economic analysis in REACH
RMOA list
ECHA's Executive Director Requests to QSAR Toolbox
the Committees Information on Candidate List
substances in articles table Mixture classification
Harmonised classification and labelling
targeted consultations REACH registration statistics UK withdrawal from the EU

Consultation on a draft C&L Inventory Recommendations to registrants


recommendation for amendment of Substances restricted under REACH
Authorisation List entries ECHA accounts and EU Login
Biocidal Active Substances Technical completeness check
Consultations in the authorisation
process Biocidal Products

List of active substances and suppliers


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Substances of very high concern Chemicals subject to PIC


identification
Transitional Measures
Occupational exposure limits - Call for
comments and evidence Information from the Existing
Substances Regulation (ESR)
Occupational exposure limits -
Previous calls for comments and PBT/vPvB assessments under the
evidence previous EU chemicals legislation

Occupational exposure limits – Candidate List


Consultations on OEL recommendation Submitted recommendations
Derogations for the protection of Adopted opinions and previous
cultural heritage consultations on applications for
Proposals for new POPs authorisation

Authorisation List

Adopted opinions on restriction


proposals

Mapping exercise – Plastic additives


initiative

Occupational exposure limits


substance evaluations

List of substances subject to POPs


Regulation

List of substances proposed as POPs

EUCLEF

European Chemicals Agency


Telakkakatu 6, P.O. Box 400, FI-00121 Helsinki, Finland Sitemap Legal Notice FOLLOW US

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