Home / Knowledge Hub Knowledge Hub Saudi Arabia Egypt UAEMedical DevicesPharmaceuticalsMedical DevicesPharmaceuticalsMedical Devices MRG Services in Saudi Arabia Requirements for Unique Device Identification (UDI) for Medical Devices Requirements for Licensing of Medical Devices Establishments Requirements for Advertisement Approval and Launching Awareness and Charity Campaigns for Medical devices Regulatory Framework for Drugs Approval Guidance on Requirements for Medical Device Listing and Marketing Authorization Requirements for Medical Devices Marketing Authorization Requirements for Post-Market Surveillance of Medical Devices Guidance Requirements Cosmetic Product Notification Classification Guidance Pharmaceuticals SFDA Regulatory Framework for Drugs Approval – Version 6.4 (2024 Update) SFDA Requirements for Formal Meetings with the Drug Sector – Version 3.1 SFDA Policy on Appeals to Drug Sector Decisions – Version 1.3 SFDA Guidelines for Investigational New Drug (IND) Requirements SFDA Updates Registration Rules for Pharmaceutical, Herbal, and Health Product Manufacturers and Their Products (Version 4) SFDA Updates Policy on Appeals to Drug Sector Decisions (Version 1.3) SFDA Updates Regulatory Framework for Drug Approval (Version 6.4) SFDA Updates Requirements for Formal Meetings Between Drug Sector and Applicants (Version 3.1) SFDA Issues Updated Guidelines on Drug Submission and Review Practices SFDA Updates Human Drug Submission Guideline (Version 4) SFDA Publishes Guideline on Good Review Practices (GRevPs) SFDA – Human Pharmaceuticals, SPC and PIL Requirements Overview of SFDA Regulatory Timelines for Pharmaceuticals and Medical Devices Ready to discuss your regulatory needs? Reach out today to begin your compliance journey with MRG.Request a consultationSchedule a meeting
Requirements for Advertisement Approval and Launching Awareness and Charity Campaigns for Medical devices
SFDA Updates Registration Rules for Pharmaceutical, Herbal, and Health Product Manufacturers and Their Products (Version 4)