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BioMed Alliance: IVDR Questionnaire

13 August 2021

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BioMed Alliance IVDR Questionnaire

On 26 May 2022 the new EU Regulation on in vitro diagnostic medical devices (the IVDR) will come into full effect, replacing the old legislation (the IVDD). This will have substantial consequences for diagnostic laboratories.

 

This means that the transition to the IVDR needs to be prepared carefully by diagnostic laboratories, including making an assay inventory. The BioMed Alliance have published a questionnaire which aims to support this preparation, in order to ensure continuity in laboratory diagnostics beyond May 2022. 

 

Your input will enable BioMed Alliance to supply you with better information and to better represent you in the process of the EU implementation of the IVDR.

 

Participants are encouraged to complete the questionnaire issued by BioMed Alliance, which can be found HERE. 

The deadline is 8 September 2021.

 

 

Alternatively please contact:  Dr. Bart Lubbers: b.r.lubbers@lumc.nl or Dr. Isabel Dombrink: Isabel.Dombrink@uksh.de for more information. 

 

Note that your contribution will be treated  as strictly confidential; laboratory- specific information will never be shared with third parties or made public.

 

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