Workshops

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

Introducing the rules for classifying the risk of medical devices

API Quality Assessment for Generic Products

Safe Handling and Disposal of Hazardous Medications

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