首页 >
法规速递
-
Page: Post-authorisation safety studies (PASS)-2025/3/25
2025-03-26查看详情 > -
Page: Industry annual bilateral meetings-2025/4/29
2025-04-30查看详情 > -
2025年6月6日中药品种保护受理公示-2025/6/6
2025-06-09查看详情 > -
Document: Article 57 product data-2025/7/15
2025-07-16查看详情 > -
Page: Accessibility-2025/8/26
2025-08-27查看详情 > -
Page: Paediatric clinical trials-2025/10/1
2025-10-08查看详情 > -
国家禁毒委员会办公室发布通告 提醒相关企业和个人防范制毒物品和非列管可制毒化学品及设备流失-2025/11/10
2025-11-11查看详情 > -
Document: Agenda - HMA/EMA Annual Data Forum 2025-2025/12/8
2025-12-09查看详情 > -
Document: Fosmetpantotenate : Notification of discontinuation of a paediatric development which is covered by an agreed PIP Decision-2026/1/19
2026-01-20查看详情 > -
Document: Data access to medicinal products for human use - Chapter 5 Annex A: Product data elements accessible by stakeholder group-2026/2/19
2026-02-27查看详情 >
