About Clinical Evaluation Report
To give a basic understanding and give some tools on how to run and benefit from the risk management process.To give an understanding of the process to run clinical evaluations and how to keep the evaluation up to date during the life cycle of a medical device.
Clinical affairs, QA/RA specialists, risk managers, marketing.
Anette Sjögren, PREVENTIA AB
Anette is a member of the Swedish (TK355 – ISO 13485, ISO 14971 and IEC 62366) and the international technical (TC210) committee and was also part of the international PMS task force.
Course material is in English.
Presentation in English or Swedish (depending on the participants).
The training is held in the area of Copenhagen, Denmark