A 4-part series on MDR
DAY & DATE Tuesday, 17th December 2020
Our expert will provide an end-to-end overview on the following topics:
All QA & Regulatory Personnel of Medical Device Manufacturers
TÜV SÜD Product Service is among the world's first certification bodies to receive designation as a Notified Body for the new Medical Device Regulation by the Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG).
As a world leader, we have worked with medical device manufacturers across the world to assess the safety and quality of their devices. Our extensive experience of conducting testing on a wide range of networked medical devices, aids your compliance to regulations and access to global markets.
With more than 750 medical device professionals in more than 30 locations worldwide, we are the largest EU Notified Body globally authorised to provide certification services under the new regulation. We have MDR / MDSAP in-country authorized auditors, with Certification across classes of devices. First Class III device approved by TÜV SÜD under MDR.
For more information, please click here.
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Bosnia and Herzegovina