Essentials of European Medical Device Regulatory Affairs - June 2020

CE Mark – Conformité European (approval for EU medical devices) CEA – Cost-effectiveness analysis CEC – Central ethics committee – but also: CEC – Commission of the European Communities CED – Coverage with evidence development CEE – Central and Eastern Europe CEEC – Central and Eastern European Countries CEFTA – Central Europe Free Trade Area CEN – Comité Européan des Normes – European Committee for Standardization CEP – Central enquiry point (MHRA) – but also: CEP – Certificate of European Pharmacopoeia (aka Certificate of Suitability) CER – Clinical evaluation report – but also: CER – Comparative effectiveness research CESP – Common European submission portal CF – Cystic fibrosis CFC – Chlorofluorocarbons CFDA – China Food and Drug Administration (formerly State FDA – SFDA ) CFR – Code of Federal Regulations (US) CFS – Certificate of Free Sale CFSAN – Center for Food Safety and Applied Nutrition (US) cGLP – Current good laboratory practice cGMP – Current good manufacturing practice CGP – Clinical Guidance Panel (Canada) CH – Clinical hold CHAI – Commission for Healthcare Audit and Inspection (UK) CHC – Consumer healthcare CHMB - Creatine kinase Muscle Brain CHMP – Committee for Medicinal Products for Human Use (EMA) CHMP – Committee for Medicinal Products for Human Use (previously: CPMP) CHO – Chinese hamster ovary cells CHPA – Consumer Healthcare Products Association CI – Confidence Interval, and also: CI – Contraindication CIA – Corporate Integrity Agreement (US) CIOMS – Council for International Organizations of Medical Sciences (WHO) CIRS – Centre for Innovation in Regulatory Science

CIS (countries) – Commonwealth of Independent States (members are former Soviet Republic countries, currently including Armenia, Azerbaijan, Belarus, Kazakhstan, Kyrgyzstan, Moldova, Russia, Tajikistan, Usbekistan,

Turkmenistan, Ukraine CK – Creatine kinase Cl – Total body clearance

Class Im – Class I with measuring function (medical devices) CLIA – Clinical Laboratory Improvement Amendments (US ) CLL – Chronic lymphocytic leukaemia CLO – Clinical overview CLP – Classification, labelling and packaging (medical devices) CLS – Clinical summary C m or C max – Maximum plasma concentration at steady state

CMA – Conditional marketing authorisation (US) CMC – Chemistry, manufacturing, and controls CMDCAS – Canadian Medical Devices Conformity Assessment System CMDh – Co-ordination Group for Mutual Recognition and Decentralised Procedures – Human (EMA) CMDR – Canadian Medical Device Regulation CMDv – Co-ordination Group for Mutual Recognition and Decentralised Procedures – Veterinary (EMA) CMN – Comité de Moléculas Nuevas” (New Molecules Committee) (Mexico) CMP – Certificate of Medicinal Product – but also: CMP – Common product model CMR – Carcinogenic, mutagenic or reprotoxic [toxic to reproduction] – but also:

CMR – Centre for Medicines Research CMS – Concerned member state (EU) CMT – Convergent medical technologies COA/CofA – Certificate of analysis