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GMP Audits
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Training
Team
Contact
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Data Privacy policy
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Data Privacy Policy
FURTHER INFORMATION
EUROPE
European Medicines Agency (EMA)
EudraLex - The Rules Governing Medicinal Products in the European Union
European Directorate for the Quality of Medicines & HealthCare (EDQM)
European Pharmacopoeia (Ph. Eur.)
European Federation of Pharmaceutical Industries and Associations (EFPIA)
USA
US Food and Drug Administration (FDA)
Code of Federal Regulations (CFR)
US Pharmacopeia (USP)
Pharmaceutical Research and Manufacturers of America (PhRMA)
Biotechnology Innovation Organization (BIO)
CANADA
Health Canada
JAPAN
Ministry of Health, Labour and Welfare (MHLW Japan)
Japan Pharmaceutical Manufacturers Association (JPMA)
AUSTRALIA
Therapeutic Goods Administration (TGA Australia)
INTERNATIONAL
World Health Organization (WHO) - Expert Committee on Specifications for Pharmaceutical Preparations
International Council for Harmonisation (ICH)
International Clinical Trials Registry Platform (ICTRP)
International Nonproprietary Names (INN)
Anatomical Therapeutic Chemical classification system and Defined Daily Dose (ATC/DDD)
International Classification of Diseases (ICD)
Orphanet - The portal for rare diseases and orphan drugs
