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Study Data Technical Conformance Guide - Technical Specifications Document-2025/3/27
2025-04-01查看详情 > -
Document: New product information wording: extracts from PRAC recommendations on signals adopted at the 7-10 April 2025 PRAC-2025/5/5
2025-05-06查看详情 > -
Document: Organisation chart: Human Medicines-2025/6/16
2025-06-17查看详情 > -
Document: Dates of 2026 Scientific Advice Working Party (SAWP) meetings and submission deadlines for scientific advice, protocol assistance, qualification of novel methodologies and HTACG/EMA parallel Joint Scientific Consultation (JSC) requests-2025/7/18
2025-07-21查看详情 > -
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 6: Examples for submission of legacy data (obsolete)-2025/9/2
2025-09-03查看详情 > -
Document: Agenda of the CVMP meeting 7-9 October 2025-2025/10/7
2025-10-08查看详情 > -
Document: Concept paper on new guidance on the clinical investigation of medicinal products for the treatment of idiopathic pulmonary fibrosis (IPF)-2025/11/13
2025-11-14查看详情 > -
Page: Medical devices-2025/12/10
2025-12-11查看详情 > -
Page: Podcast: Inside EMA-2026/1/22
2026-01-23查看详情 > -
Considerations for the use of the Plausible Mechanism Framework to Develop Individualized Therapies that Target Specific Genetic Conditions with Known Biological Cause-2026/2/23
2026-02-27查看详情 >
