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Date
2023-01-30
Guideline on good pharmacovigilance practices (GVP)
2023-01-05
Good Manufacturing Practice (GMP) Guidelines
2022-11-28
Approach of Dealing with Patents When Register Generic Drugs in SFDA
2022-11-13
Guidance for Graphic Design of Medication Packaging
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
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