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| EUDRA The European system for the authorisation of medicinal products for human and veterinary use is designed to promote both public health and the free circulation of pharmaceuticals | |
| FDA: Laws and Regulations Requirements of Laws and Regulations Enforced by the U.S. Food and Drug Administration | ||
| British Institute of Regulatory Affairs, BIRA Regulatory agency with represenation of special interest groups representing particular sectors | ||
| Code of Federal Regulations Codification of the general and permanent rules promulgated by the Executive departments and agencies of the Federal Government and published in the Federal Register. | ||
| National Institute for Biological Standards and Control, NIBSC (UK) International role in preparing, evaluating and distributing International Biological Standards and other biological reference materials | ||
| New Zealand: Ministry of Health and Information Service A group within the Ministry of Health responsible for the collection and dissemination of health-related information. | ||
| Medicines Control Agency: United Kingdom Licensing, quality inspection and enforcement. | ||
| Prescription Drug User Fee Act Related Documents (3/14/2000) This site provides documents on various user-fee related issues. | ||
| Food and Drug Administration: Clinical Trials and Treatments The agency is a cosponsor of the AIDS Clinical Trials Information Service. | ||
| European Directorate for the Quality of Medicines - European Pharmacopoeia on Responsible for monographs and guidelines, as well as the harmonization of the programs for the European community | ||
| FDA Laws Compilation of Laws Enforced by the U.S. Food and Drug Administration and Related Statutes | ||
| Australian Therapeutic Goods Administration (TGA) A national framework for regulating therapeutic drugs and devices in Australia and ensuring their quality, safety and efficacy. | ||
| FOI - FDA Medical Device Documents Using the Freedom of Information Act, we've collected over 150,000 documents that record the inner workings of the approval and regulation of medical devices, pharmaceuticals, biologics, veterinary products, foods and cosmetics. | ||
| Europa Homepage The official site of European Union. Direct links to related institutions, policies, documents and news. | ||
| Pharmacopoeia.co.uk Authoritative resource on standards for medicines in the UK | ||
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