Training Course on Post-approval Change Management of Chemical Drugs (7th Session) comes to a successful conclusion 2025-11-19

Domestic and international registration management of pharmaceutical excipients and pharmaceutical packaging materials... 2024-12-12

2.我国辅料和药包材备案登记与制剂关联审评制度 3.我国辅料和药包材管理制度发展趋势及未来展望

Domestic and international registration management of pharmaceutical excipients and pharmaceutical packaging materials... 2024-12-12

1.欧美辅料和药包材管理制度及全生命周期维护

Import registration and change maintenance of chemical APIs... 2024-12-12

已上市原料药的变更与再注册;04项目经验分享与后续政策展望

Import registration and change maintenance of chemical APIs (upper part) 2024-12-12

我国原料药审评审批制度;02进口原料药注册流程与关键节点

Requirements for the bundling review and technical evaluation of APIs, excipients and packaging materials. 2024-12-12

01 我国原辅包登记与关联审评制度简介。02原辅包登记，资料要求与常见问题;03原辅包技术审评中的常见缺陷举。