Annex 1 Manufacture of Sterile Medi

Annex 1 Manufacture of Sterile Medicinal ProductsAnnex 2 Manufacture of Biological active substances and Medicinal Products for Human UseAnnex 3 Manufacture of RadiopharmaceuticalsAnnex 4 Manufacture of Veterinary Medicinal Products other than Immunological Veterinary Medicinal ProductsAnnex 5 Manufacture of Immunological Veterinary Medicinal ProductsAnnex 6 Manufacture of Medicinal GasesAnnex 7 Manufacture of Herbal Medicinal ProductsAnnex 8 Sampling of Starting and Packaging MaterialsAnnex 9 Manufacture of Liquids, Creams and OintmentsAnnex 10 Manufacture of Pressurised Metered Dose Aerosol Preparations for InhalationAnnex 11 Computerised SystemsAnnex 12 Use of Ionising Radiation in the Manufacture of Medicinal ProductsAnnex 13 Manufacture of Investigational Medicinal ProductsAnnex 13 Detailed Commission guideline of 8 December 2017 on the good manufacturing practice for investigational medicinal products pursuant to the second paragraph of the Article 63(1) of Regulation (EU) No 536/2014Annex 14 Manufacture of Products derived from Human Blood or Human PlasmaAnnex 15 Qualification and ValidationAnnex 16 Certification by a Qualified Person and Batch ReleaseAnnex 17 Real Time Release Testing and Parametric ReleaseAnnex 19 Reference and Retention Samples