Workshops

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

Clinical Trials of Medical Device Requirements

The First Generics Scientific Evaluation

Causal survival analysis II with applications in R

Risk Management for Medical Devices: ISO 14971 Requirements

Causal survival analysis I with applications in R

National and International Experience in Regulations and Pharmacovigilance of Advanced Therapy Workshop

Herbal and Health Products Workshop: Assessment Requirements and Related Aspects

mRNA Vaccines: From Development & Regulatory Perspectives