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Rövidítés Jelentés
CABG Coronary Artery Bypass Graft
CAD Coronary Artery Disease
CADREAC Collaboration Agreement of Drug Regulatory Authorities of European…
CADRIS  Canadian Adverse Drug Reaction Information System
CANDA Computer Aided New Drug Application
CAP Color Additive Petition
CAMP  Centrally Authorised Medicinal Product
CAPIA Canadian Agency for Pharmaceutical Information Assessment
CAPLA Computer Assisted Product Licence Application
CAS Chemical Abstract Society
CBER Center for Biologics Evaluation and Research (part of US FDA)
CCC Committee of Concertation Chemistry
CCDS Company Core Data Sheet
CCP Committee of Concertation Pharmacy
CCU Coronary care unit
CD Council Direktive
CDAI Crohn's disease activity index
CDC Centers for Disease Control
CDER Center for Drugs Evaluation and Research (part of US FDA)
CDK Cyclin Dependend Kinases
CDRH Center for Devices and Radiological Health
CDSM Committee on Dental and Surgical Materials
CdT Translation Center for the Bodies of the EU (Luxemburg)
CEC Commission of the European Communities
CEE  Central and Eastern Europe
CEO  Chief Executive Officer
CES Clinical Expert Statement
CEX Excipient control method
CFR  Code of Federal Regulations (USA)
CGMP Current Good Manufacturing Practice
CGMP Certificate of Good Manufacturing Practices
CGRM Calcitonine Gene Related Peptide
CHD Coronary Heart Disease
CHE Cholinestarase
CHF Congestive Heart Failure
CHF Cardiac Heart Failure
CHMP Committee for Medicinal Products for Human Use
CI Confidence interval
CIB Clinical Investigator Bochure
CIDS Canadian Implantable Defibrillator Study
CIOMS Council for International Organisations of Medical Sciences
CIOMS  Council for International Organizations of Medical Sciences
CJD Creutzfeldt-Jakob Disease
CK-MB Creatine Kinase MB Band
CL Clearence
CLD Certain Lethal Dose
CMC Chemistry, Manufacturing and Control
CMD(h)  Coordination group for Mutual recognition and Decentralised procedures (human)
CMD(v)  Coordination group for Mutual recognition and Decentralised procedures (veterinary)
CMR Centre for Medicines Research (international, based in the UK)
CNS Central Nervous System
CoA Certificate of Analysis
COMP Commitee for Orphan Medicinal Products
COPD Chronic Obstructive Pulmonary Disease
COSTAR Dictionary used to code adverse experiences
COSTART Codification of Standard Terminology of Adverse Reactions Terms (USA)
CPA Active Ingredient control method
CPAC Central Pharmaceutical Affairs Council (JAPAN)
CPF Finished product control method
CPK Creatine Phosphokinase
CPMP Committee for Proprietary Medicinal Products (EC)
CPP Certificate of Pharmaceutical Product
CPR Cardiopulmonale Reanimation
CPSC Consumer Product Safety Commission
CPT  Consumer Project for Technology
CRA Clinical Research Associate
CRF Case Report Form
CRM Committee on the Review of Medicines
CRO Contract Research Organisation
CRO Clinical Research Organization
CRS Chemical Reference Substance
CRT Case Report Tabulation
CRU Clinical Research Unit
CTA Clinical Trials Applications
CTC Clinical Trial Certificate
CTD Commulative Trauma Disorder
CTD Clinical Trials Directive
CTD Common Technical Document
CTFG Clinical Trial Facilitation Group
CTG CardioTokoGraph
CTM Clinical Trial Management
CTS  Communication and Tracking System
CTX Clinical Trial Exemption
CV CardioVersion
CV Curriculum Vitae
CVM Center for Veterinary Medicine
CVMP Committee for Veterinary Medicinal Product (EC)
CY  Cyprus
CZ  Czech Republic
CCSI Company Core Safety Information
CSI Core Safety Information
CSM Committee on Safety of Medicines
CSO Consumer Safety Officer

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