Skip to main content
Date
2025-10-30
Guidance on Submission of Chemistry, Manufacturing, and Control (CMC) Information for Human Gene Therapy Clinical Trial Application
2025-10-21
Economic Evaluation Studies Guidelines
2025-10-08
Approach of Dealing with Patents When Register Generic Drugs in SFDA
2025-09-30
Guideline for Testing of Residual Formaldehyde
2025-08-20
Guideline on good pharmacovigilance practices (GVP)
2025-08-12
User Manual for Traveler Clearance Controlled Drug System
2025-08-05
Guidance for Veterinary Good Clinical Practice VICH GL9
2025-08-04
Testing of Residual Moisture
عرض 1 - 9 من 107