Medidee Services SA
The Leading European Consultancy Service exclusively supporting Medical Devices and In-Vitro Diagnostics compliance with international regulatory requirements
Medidee provides expertise for validation and market introduction of:
Our services cover all quality, regulatory and clinical activities required at each steps of a medical device lifecycle, from the initial project idea to certification or regulatory clearance. We support our customer in ensuring regulatory requirements are efficiently implemented and contribute to the interactions with regulatory bodies
Based in Switzerland, Denmark, Germany and USA, we are active in Europe, Asia, Australia and both North and South America.
We provide extended information and material to facilitate the regulatory process for our customers. Medidee is ISO 9001 and ISO 13485 certified.
Please contact us at: firstname.lastname@example.org
Please visit us at www.medidee.com
+41 21 311 20 59