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Document: PMF dossier requirements - Questions and answers for PMF holders-2025/5/14
2025-05-15查看详情 > -
Document: Article 57 product data-2025/6/23
2025-06-24查看详情 > -
Document: Substances considered as not falling within the scope of Regulation (EC) No. 470/2009, with regard to residues of veterinary medicinal products in foodstuffs of animal origin-2025/7/25
2025-07-27查看详情 > -
Alternative Tools: Assessing Drug Manufacturing Facilities Identified in Pending Applications-2025/9/11
2025-09-12查看详情 > -
Page: Scientific publications-2025/10/15
2025-10-16查看详情 > -
图解海报 | 《国家药监局关于深化化妆品监管改革促进产业高质量发展的意见》系列解读(五)-2025/11/20
2025-11-21查看详情 > -
Document: European Medicines Agency post-authorisation procedural advice for users of the centralised procedure: document with tracked changes-2025/12/15
2025-12-16查看详情 > -
Page: Quality of medicines questions and answers: Part 1-2026/1/28
2026-01-29查看详情 > -
Document: Opinion of the CVMP on the establishment of maximum residue limits: Fluralaner ( EMEA/V/MRL/004380/EXTN/0002)-2026/3/6
2026-03-09查看详情 > -
Document: Highlights - EMA - European Alliance of Associations for Rheumatology (EULAR) bilateral meeting - March 2026-2026/4/7
2026-04-08查看详情 >