CLINICAL TRIAL REGISTRIES
EU Post-Authorisation Studies (EU-PAS) Register
National Institutes of Health Clinical Trials Database
CRO & CRA ASSOCIATIONS
Association of Clinical Research Organizations (ACRO)
European CRO Federation (EUCROF)
Society of Clinical Research Associates (SoCRA)
REGULATORY AGENCIES FOR THE EVALUATION OF MEDICINAL PRODUCTS
European Medicines Agency (EMA)
Heads of Medicines Agencies (HMA)
US Food and Drug Administration (US FDA)
REGULATIONS & GUIDELINES
Council for International Organizations of Medical Sciences (CIOMS)
Declaration of Helsinki, World Medical Association
European Directorate for the Quality of Medicines & Healthcare
European Federation of Pharmaceutical Industries and Associations (EFPIA)
European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP)
Good Clinical Practices (GCP) ICH Guidelines
Good Distribution Practices (GDP) EU Guidelines
Good Laboratory Practice (GLP) OECD Guidelines
Good Manufacturing Practice (GMP) EU Guidelines
Good Pharmacoepidemiology Practices (GPP) ISPE Guidelines
Good Pharmacovigilance Practices (GVP) EU Guidelines
Post-Authorisation Safety Studies (PASS)
MEDICAL DICTIONARIES/CODING
Medical Dictionary for Regulatory Activities (MedDRA)
WHO Collaborating Centre for Drug Statistics Methodology, ATC/DDD Index
REPORTING OF CLINICAL STUDIES
Enhancing the QUAlity and Transparency Of health Research (EQUATOR)
Committee on Publication Ethics (COPE)
Consolidated Standards of Reporting Trials (CONSORT)
International Committee of Medical Journal Editors (ICMJE)
STrengthening the Reporting of OBservational studies in Epidemiology (STROBE)