Guidelines

Date
2023-06-01
Drugs Guide
Guideline on the Braille Requirements for Labeling Information of Medicinal Products for Human Use
2023-04-04
Drugs Guide
Guidance on Submission of Chemistry, Manufacturing, and Control (CMC) Information for Cell-based Clinical Trial Applications
2023-03-29
Drugs Guide
Specifications: Test Procedures and Acceptance Criteria for New Veterinary Drug Substances and New Medicinal Products: Chemical Substances (VICH GL39)
2023-01-30
Drugs Guide
Guideline on good pharmacovigilance practices (GVP)
2023-01-05
Drugs Guide
Good Manufacturing Practice (GMP) Guidelines
2022-11-28
Drugs Guide
Approach of Dealing with Patents When Register Generic Drugs in SFDA
2022-11-13
Drugs Guide
Guidance for Graphic Design of Medication Packaging
2022-11-13
Drugs Guide
Guidance on Publication of Public Assessment Reports for Medicinal Products for Human Use (Saudi-PAR)
2022-11-09
Drugs Guide
Guidance for the Preparation of a Site Master File (SMF)
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