New training will be organized in Q4 2022
This full-day training workshop will be a great introduction to Medical Device Regulation and Quality Management System requirements according to EN ISO 13485:2016. This will help you gain in-depth knowledge on key topics, supporting your current or future development. Take a look at the detailed agenda below.
Reviews of previous participants:
“Helped us with making the daunting MDR and QMS requirements more approachable and less abstract. (10/10)”