Conference & Workshop
No.
Title
Date
1
Elements of a Successful Registry in the Post-Market Surveillance System
2013-01-11
2
Development and Implementation of a Medical Device Post-Market Surveillance System - The Chinese Taipei Experience
3
Enhancement of Post-Market Surveillance -Experience in the EU
4
Overview of Global Issues and Activities Related to Counterfeit/Falsified Medical Products
5
Medical Device Quality Management System
6
The IAF Initiative for Accredited Certification of ISO 13485 Part III
7
The IAF Initiative for Accredited Certification of ISO 13485 Part II
8
The IAF Initiative for Accredited Certification of ISO 13485 Part I