首页 >
法规速递
-
Document: EU Implementation Guide (IG) on veterinary medicines product data in the Union Product Database - Chapter 2: Format for the electronic submission of veterinary medicinal product information-2025/5/21
2025-05-22查看详情 > -
Document: Scientific recommendations on classification of advanced therapy medicinal products-2025/5/21
2025-05-22查看详情 > -
Document: Appendix 1: Acceptable intakes established for N-nitrosamines-2025/5/21
2025-05-22查看详情 > -
Document: Agenda - PDCO agenda of the 20-23 May 2025 meeting-2025/5/20
2025-05-21查看详情 > -
Page: Electronic product information (ePI)-2025/5/20
2025-05-21查看详情 > -
Document: Nitrosamines EMEA-H-A5(3)-1490 - Questions and answers for marketing authorisation holders / applicants on the CHMP Opinion for the Article 5(3) of Regulation (EC) No 726/2004 referral on nitrosamine impurities in human medicinal products-2025/5
2025-05-20查看详情 > -
Document: Standard operating procedure for validation, publication, and maintenance of real-world data sources and studies in the HMA-EMA RWD Catalogues-2025/5/19
2025-05-20查看详情 > -
Document: European Medicines Agency’s Data Protection Notice for the Organisation Management System (OMS) activities-2025/5/19
2025-05-20查看详情 > -
Document: Records of data processing activity for the Organisation Management System (OMS) activities-2025/5/19
2025-05-20查看详情 > -
Document: CTIS newsflash - 16 May 2025-2025/5/19
2025-05-20查看详情 >