Major GMP Guidlines
EU GMP Annex 1: Manufacture of Sterile Medicinal Products
EU GMP Annex 2: Manufacture of Biological Medicinal Products for Human Use
EU GMP Annex 3: Manufacture of Radiopharmaceuticals
EU GMP Annex 4: Manufacture of Veterinary Medicinal Products other than Immunolo ...
EU GMP Annex 5: Manufacture of Immunological Veterinary Medicinal Products
EU GMP Annex 6: Manufacture of Medicinal Gases
EU GMP Annex 7: Manufacture of Herbal Medicinal Products
EU GMP Annex 8: Sampling of Starting and Packaging Materials
EU GMP Annex 9: Manufacture of Liquids, Creams and Ointments
EU GMP Annex 10: Manufacture of Pressurised Metered Dose Aerosol Preparations fo ...
EU GMP Annex 11: Computerised Systems
EU GMP Annex 12: Use of Ionising Radiation in the Manufacture of Medicinal Produ ...
EU GMP Annex 13: Investigational Medicinal Products
Detailed Commission guidelines on good manufacturing practice for investigationa ...
EU GMP Annex 14: Manufacture of Products derived from Human Blood or Human Plasm ...
EU GMP Annex 15: Qualification and Validation
EU GMP Annex 16: Certification by a Qualified Person and Batch Release
EU GMP Annex 17: Real Time Release Testing and Parametric Release
EU GMP Annex 19: Reference and Retention Samples