Top Industry News
- Swissmedic- Public Review of the New eCTD M1 Specification v1.5
- ANVISA- Drug Registration Grows 100%
- SFDA- Draft of Regulatory Framework for Drugs Approval
- FDA- Bridging for Drug-Device and Biologic-Device Combination Products
- SFDA- Data Requirement for Herbal & Health Products Submission
- European Medicines Agency Post-Authorisation Procedural Advice for Users of the Centralised Procedure
- SFDA- Guidance on SFDA Recognized Standards
- Swissmedic and the Korean Agency for Therapeutic Products Expand their Cooperation in the Area of Medicinal Products
- SFDA- Guidance on Innovative Medical Devices