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SFDA’s CEO Meets with President of German Paul-Ehrlich-Institut News

SFDA Explores Cooperation Opportunities with Irish National Institute for Bioprocessing Research and Training News

Sahl Almadar service providing facilities

Semi-annual PV Inspection report 2022 Awareness Article

Dr. Aljadhey Heads Saudi Delegation Participating in ICMRA Summit in Ireland News

Conditional Approval for Medicinal Products for Human Use Regulations

(WU2247) NCMDR Weakly Update Medical Report

Guidance on Publication of Public Assessment Reports for Medicinal Products for Human Use (Saudi-PAR) Regulations

Post-market clinical evaluation for the Safety and the Current Local Practices of Ultrasound Gel Products Medical devices studies

Requirements for Post-Market Surveillance of Medical Devices (MDS – REQ11) Regulations