Workshops

Advanced Pharmacovigilance: Enhancing Regulatory Practices and Digital Integration

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