ISO 13485:2016 QUALITY MANAGEMENT SYSTEM FOR MEDICAL DEVICES

Greetings from the Medical Device Authority!

We would like to announce that MDA will be conducting a training program.

This workshop provides a face-to-face platform for medical device establishments, medical device industry representatives, conformity assessment bodies, and stakeholders to have an in-depth understanding ISO 13485:2016 Quality Management System for Medical Devices.

This workshop specifically will help industry in understanding the ISO 13485:2016 which serves as an international standard for manufacturers to provide medical devices and related services that consistently meet customer needs and applicable regulatory requirements.

This Workshop will benefit all relevant stakeholders who are involved with medical devices including:
• Manufacturers, authorized representatives, importers, and distributors;
• Medical device industry representatives;
• Designated persons; and
• Interested individuals

Registration is now open until 5th December 2023. Please register at:
https://docs.google.com/forms/d/12VL4Yg-ZvodDw3svg-9Yh6nVwAgI7rwaFa0ll8A-rjY/edit?ts=655db209
Or you may scan the QR Code from the poster.
For further inquiries, please reach out to us via email at:
[email protected]
cc:[email protected]

Thank you.