Workshops

Medical Device Clinical Evaluation File

Requirements for biological evaluation and biocompatibility of medical devices and medical supplies

Good Clinical Practice (GCP) Foundation Course Agenda

Risk Management for Software as a Medical Device and AI-enabled Medical Device

Medical Device Clinical Trials

SFDA’s regulatory oversight and the role of Conformity Assessment Bodies

Overview of Pharmaceutical Manufacturing Inspections and Key observations

Software as a Medical Device Verification and Validation

Saudi Unique Device Identification (SAUDI-DI) for medical devices Requirements & Submission process