UK

• Medicines and Healthcare products Regulatory Agency (MHRA)
• MHRA Medicines Section
• MHRA Medicines Section - MAIL
• MHRA Medicines Section - Recalls/DMRC
• MHRA Medical Devices Section
• Veterinary Medicines Directorate (DEFRA)
• National Institute for Biological Standards and Control
• UK Statutory Instruments

USA

• Food and Drug Administration (FDA) Home Page
• FDA - Centre for Biologics Evaluation and Research
• FDA - Centre for Drug Evaluation and Research
• FDA - Code of Federal Regulations
• FDA - Inspection References: Index
• FDA - Inspection Guides
• FDA - Guidance Documents: Index
• FDA - Warning Letters - General Searches

Pharmaceutical Inspection Co-operation Scheme

• PICS

Australia

• Therapeutic Goods Administration

Jargon Buster

• Jargon Buster Document

Europe

• European Medicines Agency (EMEA)
• "Eudralex" Rules Governing Medicinal Products In The EU
• Quality Working Party Guidelines - for EU Marketing Authorisation Applications
• EMEA Inspections Homepage
• EU Inspectorates - What's New
• GMP Sector of the EMEA Site

Qualified Person

• Guidance Notes to Assist the QP
• Royal Society of Chemistry
• Institute of Biology
• Royal Pharmaceutical Society of Great Britain

International Conference On Harmonisation

• International Conference on Harmonisation (ICH) Home Page

WHO - World Health Organisation

• WHO

Pharmacopoeias

• US Pharmacopoeia
• European Pharmacopoeia (EDQM)
• British Pharmacopoeia

Risk Assessment

• Risk Assessment