Courses #medical devices - Eventura World

Developing Effective Post Market Surveillance and Complaint Handling Requirements (Interrelationship with CAPA, Change Control, Adverse Event Reporting and Recalls)

Good Manufacturing Practices (GMP) 101

FDA Inspections Seminar for 2024

Risk Management for ML Medical Devices following AAMI/ BSI TR 34971 and ISO 14971

4-Hour Virtual Seminar On Usability Principles For Medical Devices: Interpreting And Implementing IEC 62366

MedReg 2023 - Annual Medical Device Regulatory Confex

Production and Process Controls for Medical Devices

QUALITY & REGULATORY PATHWAYS FOR SAMD & AI DEVICES – ALL YOU NEED TO KNOW

COMPLAINT HANDLING, MEDICAL DEVICE REPORTING AND RECALLS - POST-MARKET REGULATIONS TRAINING