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British Pharmacopoeia (BP) Canadian HPFB Inspectorate European Chemical Industry Council - Active Pharmaceutical Ingredients Sector (CEFIC/APIC) The European Commission DG Enterprise European Compilation of Procedures for GMP Inspections European Federation of Pharmaceutical Industries and Federations (EFPIA) European Guide to GMP European Guide to GMP - updates etc European Guidelines on Quality, Safety, and Efficacy European Medicines Agency (EMEA) European Medicines Agency Inspections Sector European Pharmacopoeia (EP) Food and Drug Administration (FDA) FDA CBER Guidance / Guidelines / Points to Consider FDA GMP Regulations (CFR21) FDA Inspections Operations Manual FDA Inspection Guides FDA portal providing access to the different parts of their website Good Automated Manufacturing Practice (GAMP) Health Sciences Authority (HSA) - Singapore International Conference on Harmonisation (ICH) International Pharmaceutical Excipients Council (IPEC) International Pharmaceutical Federation (FIP) International Society for Pharmaceutical Engineers (ISPE) Irish Medicines Board (IMB) Japanese Ministry of Health, Labour and Welfare (MHW) Malaysian National Pharmaceutical Control Board (NPCB) Medical Device Link Mutual Recognition Agreements (MRAs) The Parenteral Society - UK Pharmaceutical Inspection Cooperation Scheme (PIC/S) Pharmaceutical Online Pharmaceutical and Research Manufacturers of America (PhRMA) The Pharmaceutical Quality Group (PQG) Pharmacos Enterprise DG PharmWeb Regsource - Regulatory Information Risk-Based Approach to Pharmaceutical Current Good Manufacturing Practices (cGMP) for the 21st Century - Table of Contents Therapeutic Goods Administration (TGA) - Australia Therapeutic Products Directorate - Canada UK Medicines and Healthcare Products Regulatory Agency (MHRA) UK Official Documents including the "Orange Guide" and Medicines Legislation United States Pharmacopoeia (USP) World Health Organisation GMP Information (WHO) World Pharma Web |
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