Workshops

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

Requirements for Clinical Trials of Medical Devices

Medical Devices Marketing Authorization (MDMA) Requirements for Spectacles lenses

Real-World Evidence for Post-Marketing Regulatory Decisions

Assessment and Classification of Herbal and Health Products: Webinar

Artificial Intelligence (AI) and Machine Learning (ML) medical devices regulatory approach