| Annex 1 |
Manufacture Of Sterile Medicinal Products |
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| Annex 2 |
Manufacture Of Biological Medicinal Products For Human Use |
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| Annex 3 |
Manufacture Of Radiopharmaceuticals |
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| Annex 4 |
Manufacture Of Veterinary Medicinal Products Other Than Immunological Veterinary Medicinal Products |
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| Annex 5 |
Manufacture Of Immunological Veterinary Medicinal Products |
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| Annex 6 |
Manufacture Of Medicinal Gases |
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| Annex 7 |
Manufacture Of Herbal Medicinal Products |
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| Annex 8 |
Sampling Of Starting And Packaging Materials |
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| Annex 9 |
Manufacture Of Liquids, Creams And Ointments |
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| Annex 10 |
Manufacture Of Pressurised Metered Dose Aerosol Preparations For Inhalation |
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| Annex 11 |
Computerised Systems |
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| Annex 11 (Updated) |
Computerised Systems - For review and comment |
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| Annex 12 |
Use Of Ionising Radiation In The Manufacture Of Medicinal Products |
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| Annex 13 |
Manufacture Of Investigational Medicinal Products |
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| Annex 14 |
Manufacture Of Medicinal Products Derived From Human Blood Or Plasma |
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| Annex 15 |
Qualification And Validation |
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| Annex 15b |
Validation Master Plan Design Qualification, Installation And Operational Qualification Non-Sterile Process Validation Cleaning Validation |
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| Annex 16 |
Certification By A Qualified Person And Batch Release |
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| Annex 17 |
Parametric Release |
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| Annex 18 |
Good Manufacturing Practice For Active Pharmaceutical Ingredients |
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| Annex 19 |
Reference And Retention Samples |
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| Annex 20 |
Quality Risk Management |
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| GDP Guide |
Good Distribution Practice Guideline |
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