Workshops

Saudi Unique Device Identification (SAUDI-DI) for Medical Devices Requirements & Submission Process

Companion Diagnostic Regulatory Requirements

Medical Device Clinical Evaluation File

Good Clinical Practice (GCP) Foundation Course Agenda

Clinical trials Requirements of Medical Device

Analytical and clinical performance requirements for IVDs

Model Based Drug Development ( ICH M15 Updates) Virtual Symposium

Medical Devices Marketing Authorization (MDMA) Requirements for Spectacles lenses Requirements

Point of Care Manufacturing and In-House IVDs