Workshops

Medical Devices Marketing Authorization (MDMA) Requirements for Contact lenses and Contact lenses solutions.

Risk Management for Medical Devices

What's new in The Guideline on Quality Considerations for Development and Comparability Assessment of Biosimilars

Implementing the One Health Approach to Combat Antimicrobial Resistance

Manufacturing medical devices at Points of Care (POC)

Regulatory Considerations and Localization of CAR T-Cell Therapy

Risk Management for Medical Devices: ISO 14971 Requirements

API Quality Assessment for Generic Products

Introducing the rules for classifying the risk of medical devices