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Date
2022-11-13
Guidance on Publication of Public Assessment Reports for Medicinal Products for Human Use (Saudi-PAR)
2022-11-09
Guidance for the Preparation of a Site Master File (SMF)
2022-11-09
Guideline on Blood Products (Plasma Derived Medicinal Products)
2022-11-06
Data Requirements for Veterinary Medicinal Products
2022-10-13
The Data Requirements for Human Drugs Submission
2022-09-12
Stability Testing of New Veterinary Drug Substances
2022-09-12
Guideline on the Conduct of Bioequivalence Studies for Veterinary Medicinal Products
2022-08-25
Contract Research Organization Guideline
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