31
/
Oct
Training New MDR Regulation 2017/745 on Medical Devices: technical file structure
9:00 AM - 11:00 AM
Online
Regulation 745/2017 on Medical Devices: technical file structure Duration: 1 hours Prerequisite: basic knowledge of medical devices and regulatory requirements in Europe Recipients: Quality Assurance, Regulatory, Top Management of companies…
24
/
Jan
Live Webinar: Drafting of the Biocompatibility report in accordance with ISO 10993-1
9:00 AM - 12:00 PM
Online
The course is aimed at staff of Quality Assurance, Regulatory, and research and development of biomedical companies legalii manufacturers of medical devices of any class, who are in contact with…
13
/
Dec
Live Webinar Validation of industrial processes (IQ/OQ/PQ) and technology transfer in accordance with ISO 13485: 2016
9:00 AM - 12:00 PM
Online
The course is aimed at Quality Assurance personnel, Regulatory, Production and Research & Development of biomedical companies and legal medical device manufacturers of any class.