About Clinical Evaluation Report
Goal:
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.
Who benefits:
Clinical affairs, QA/RA specialists, risk managers, marketing.
Course Leader:
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.
Language:
Course material is in English.
Presentation in English or Swedish (depending on the participants).
Venue:
The training is held in the area of Copenhagen, Denmark