Workshops

Good Clinical Practice (GCP) Foundation Course Agenda

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

Medical Device Clinical Trials

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

Medical Device Clinical Evaluation File

Risk classification for Medical Devices

SFDA Efforts on Advancing Biosimilars Development and Regulation: Understanding the New Regulatory Framework