首页 >
法规速递
-
Document: Product Management Service (PMS) User Acceptance Testing (UAT) Application Programming Interface (API) registration process for industry - Chapter 1, Annex A-2026/6/12
2026-06-15查看详情 > -
Formal Meetings Between FDA and ANDA Applicants of Complex Products Under GDUFA Guidance for Industry (Final)-2022/10/5
2022-11-15查看详情 > -
Draft Guidance: Assessing Adhesion With Transdermal and Topical Delivery Systems for ANDAs Draft Guidance for Industry-2023/4/12
2023-04-13查看详情 > -
《国家药监局关于化学原料药再注册管理等有关事项的公告》政策解读-2023/10/13
2023-10-13查看详情 > -
Page: Ethical use of animals in medicine testing-2025/1/8
2025-01-09查看详情 > -
Document: QRD veterinary product-information highlighted template version 9.1-2025/2/14
2025-02-18查看详情 > -
Page: Type-IA variations: questions and answers-2025/3/25
2025-03-26查看详情 > -
Page: Human papillomavirus (HPV)-2025/4/28
2025-04-29查看详情 > -
Document: Guidance on the details of the classification of variations requiring assessment according to Article 62 of Regulation (EU) 2019/6 for veterinary medicinal products and on the documentation to be submitted pursuant to those variations-2025/6/5
2025-06-06查看详情 > -
国家药监局关于批准注册225个医疗器械产品的公告(2025年6月)(2025年第67号)-2025/7/15
2025-07-16查看详情 >
