Specificities of active implantable medical device (AIMD) development
The Medi'Nov Connection trade show brings together the key players in the world of medical devices. In addition to the conferences and exhibition hall,...
The medical regulatory environment is changing rapidly, particularly in Europe with the arrival of Regulation 2017/745. As a regulatory manufacturer, your approval files must be updated. Do you have a need to assemble and/or update your approval files?
Cisteo MEDICAL offers you regulatory support by putting at your service the experience of our Regulatory Affairs Manager, Ms. Elise WALLART and her team, to anticipate and pass this evolution without stress. It will be a real pleasure to collaborate together in this increasingly demanding regulatory context.
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