All medical devices sold in Europe must comply with relevant medical device regulations. The Technical Documentation is your proof of compliance. In this course, you will get to know more about how to avoid common mistakes and how to speed up the process of review and CE marking.
You will learn more about the requirements on technical documentation and what is expected from you as a manufacturer. After the course you will have the tools you need for managing a smooth third-party review and to avoid common mistakes.
SEK 3 900:- for participants from member companies to Swedish Medtech
SEK 4 400:- for non-members
Course material will be in English, verbal presentation and discussions in Swedish.