Getting ready for the IVDR transition: Information request form

Thermo Fisher Scientific is committed to supporting clinical laboratories across the EU in preparation for the transition to In Vitro Diagnostic Regulation (IVDR) (EU) 2017/746. For more information about the transition or products under development, please contact the Thermo Fisher Scientific transition team (please specify in the subject line the specific nature of your inquiry).

To stay up to date on clinical testing solutions for infectious diseases and receive updates on IVDR information from Thermo Fisher Scientific, please fill out the form below.

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