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Document: FAQs: Introduction to the Clinical Trials Regulation (EU) No 536/2014 - CTIS Training Programme - Module 01-2025/2/18
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Document: European Medicines Agency’s data protection notice regarding personal data processing in the Clinical Trials Information System (CTIS)-2025/2/18
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Page: Maximum residue limits (MRL)-2025/2/18
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Document: Agenda - ACT EU workshop on ICH E6 (R3)-2025/2/18
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Document: Programme - EMA's Open Door Day-2025/2/18
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Document: Minutes - HMA-EMA joint Big Data Steering Group teleconference - 11 December 2024-2025/2/17
2025-02-18查看详情 > -
Page: International Coalition of Medicines Regulatory Authorities (ICMRA)-2025/2/17
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Document: Agenda of the COMP meeting 18-19 February 2025-2025/2/17
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Document: New product information wording – Extracts from PRAC recommendations on signals adopted at the 28-31 October 2024 PRAC-2025/2/17
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Page: Big data-2025/2/17
2025-02-18查看详情 >