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Regulatory Affairs Medtech
Stakeholders support exemption of in-house IVDs from EU directive, with conditions
01 March 2011
Amanda Maxwell

Respondents to the European Commission's consultation on the proposed revision of the In Vitro Diagnostic Devices Directive (98/79/EC) have said that if "in-house tests" were no longer exempt from the directive, patients would suffer from the lack of availability of certain much-needed diagnostic tests

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