Workshops

Risk Management for Medical Devices: ISO 14971 Requirements

Overview on the new SFDA IT Service Overseas Medical Devices Manufacturer Account

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

Biotechnology and Innovation in Medical Devices industry

Introducing The Rules for Classifying The Risk of Medical Devices

Product Sterilization Requirements for Medical Devices

Clinical Trials of Medical Device Requirements

Contact Lenses and Solutions Technical Requirements

Manufacturing medical devices at Points of Care (POC)