TÜV SÜD Product Service becomes fourth Notified Body under IVDR
As announced by TÜV Süd Product Service GmbH on 17 June 2020, the German Central Authority of the Länder for Health Protection with regard to Medicinal Products and Medical Devices (ZLG) designated the company as the fourth Notified Body according to the In Vitro Diagnostic Regulation (IVDR).
In addition to the IVDR, TÜV SÜD is one of the few Notified Bodies also designated under the In Vitro Diagnostic Directive (IVDD). As the world's largest Notified Body for medical devices and in-vitro diagnostics introduced on the market in the European Economic Area the company has already strengthened its international team.
Source:
TÜV SÜD: Press release
Meet the GMP Compliance Adviser
The GMP Compliance Adviser is the world's largest knowledge portal for quality management in the pharma business.
The demo access is non-binding and ends automatically.
You may also be interested in the following articles:
