IVD TRIALS – Your German partner for high-quality trials. 
With our expert team and numerous test systems, we perform the entire validation process for you at our own facilities.
Take advantage of our extensive know-how in analytical and clinical validation, compliant with the EU IVDR, WHO, TGA or Chinese NMPA.
Our study offerings include clinical and analytical performance evaluations for all major methods such as PCR, rapid tests and immunoassays (CLIA), including usability studies, e.g. laymen studies (self-testing), and near patient testing (PoC, Point-Of-Care).

Are you looking to validate your IVD products according to EU IVDR?
This is why our experts guarantee the best chances for an approval of your assay:
- 100% in-house expertise, no freelancers or subcontractor
- Direct access to more than 900,000 human biospecimens in stock as part of the German MEX Group
- 250 proven record from more than 250 successful clinical IVD trials at highest quality levels

IVD TRIALS

The Hans-Bunte Straße 6 office in Heidelberg focuses on clinical study management and site coordination for research projects.

IVD TRIALS

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