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EU's classification matrices for MDD
EU's classification matrices for IVD
Study on “Development of enforcement indicators for REACH and CLP” - Final Report
CLP Regulation - Study on the harmonisation of the information to be submitted to Poison Centres, according to article 45 (4) of the Regulation (EC) No 1272/2008
Instructions - Access to CARACAL papers publicly available in CircaBC - REACH - CLP
WORKING DOCUMENT on the main text and Annex I of the CLP Regulation (EC) No 1272/2008 consolidated version with Regulation (EC) No 487/2013 (4th ATP to CLP)
Manual on borderline and classification in the community regulatory framework for medical devices
Review of the functioning of the CPV codes/system
Chemicals - Poison centres - Harmonisation of Information for Poison Centres - Review according to Article 45(4) of Regulation (EC) No 1272/2008 on classification, labelling and packaging of substances and mixtures
Chemicals - Commission review for the harmonisation of information relating to emergency health response (Art. 45 CLP Poison Centres)
Guidance document - In vitro diagnostic medical devices - Borderline and Classification issues. A guide for manufacturers and notified bodies - MEDDEV 2.14/1 rev.2
Guidance document Medical Devices - Scope, field of application, definition - Qualification and Classification of stand alone software - MEDDEV 2.1/6
Guidance document - Classification of Medical Devices - MEDDEV 2.4/1 rev.9
CLP Fee Regulation
Chemicals - Classification - CLP Fee Regulation
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