MEDOTEC AB
Expert regulatory partner for medical device clinical compliance assessments.
Översikt
- Okänt
- Anställda
- Okänt
- Omsättning
- 2020
- Grundat
Beskrivning
MEDOTEC AB functions as a specialized regulatory partner focusing on the complex requirements introduced by the EU Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR). They primarily serve other businesses, including medical device manufacturers, Notified Bodies, and regulatory...