About
This program provides a comprehensive guide to implementing and maintaining a Quality Management System based on the ISO 13485:2016 standard. Designed specifically for organizations involved in the design, production, installation, and servicing of medical devices, the course covers regulatory requirements, risk management, and process control. Participants will learn how to align their operations with international safety and quality expectations to ensure compliance and improve patient outcomes through consistent product safety and efficacy.
You can also join this program via the mobile app. Go to the app
Overview
Price
R 999,00
Group Discussion
This program is connected to a group. You’ll be added once you join the program.
ISO 13485: Quality Management for Medical Devices
Private1 Member