FOCUS: Clinical evaluation of your medical device
Clinical evaluation is a mandatory step in the process of obtaining CE marking for a medical device.
Excerpt from the press release of September 21, 2020
Cisteo MEDICAL, specializing in the development and manufacturing of medical devices under contract, is launching Cisteo CONSULTING, a new regulatory and standards consulting activity.
Cisteo CONSULTING supports medical device manufacturers in their medical device approval process and in the management of their ISO 13485 quality system.
This new activity will be presented as part of the DM Back to School event which will be held in Besançon on September 29 and 30, 2020, but also at the MedTech Meetup trade fair in Brussels on October 2, 2020.
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