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Page: Transfer of marketing authorisation: questions and answers-2026/7/13
2026-07-14查看详情 > -
Page: Guidance on good manufacturing practice and good distribution practice: Questions and answers-2026/7/13
2026-07-14查看详情 > -
Page: Extensions of marketing authorisations: questions and answers-2026/7/13
2026-07-14查看详情 > -
Page: Post-authorisation safety studies (PASS)-2026/7/13
2026-07-14查看详情 > -
Page: Worksharing: questions and answers-2026/7/13
2026-07-14查看详情 > -
Page: Type-II variations: questions and answers-2026/7/13
2026-07-14查看详情 > -
Page: Type-IB variations: questions and answers -2026/7/13
2026-07-14查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure-2026/7/13
2026-07-14查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2026/7/13
2026-07-14查看详情 > -
Document: Scientific recommendations on classification of advanced therapy medicinal products-2026/7/10
2026-07-11查看详情 >
