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Glossary of regulatory terms

EMA's glossary of regulatory terms gives definitions for the main regulatory terms used on this website and in EMA documents.

EMA has developed the definitions in this glossary to help this website's users understand regulatory terminology. Definitions may differ from those given in European Union legislation.

You can search within this glossary or click on a letter below to see terms beginning with that letter.

C

CAT
Centralised procedure
Centrally authorised product
CHMP
Class waiver
Clinical trial
Clock stop
CMDh
CMDv
Co-rapporteur
Commercially confidential information
Committee for Advanced Therapies
Committee for Medicinal Products for Human Use
Committee for Orphan Medicinal Products
Committee for Proprietary Medicinal Products
Committee for Veterinary Medicinal Products
Committee on Herbal Medicinal Products
Common technical document
COMP
Compassionate use
Competent authority
Concept paper
Concerned Member State
Conditional marketing authorisation
Coordination Group for Mutual Recognition and Decentralised Procedures - Human
Coordination group for mutual recognition and decentralised procedures for veterinary medicinal products
Counterfeit medicine
CVMP