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New HemaSphere publication on IVDR implementation
The In Vitro Diagnostic medical devices Regulation (IVDR), which came in to force in May 2022 with the objective of safeguarding the quality and safety of diagnostic tests in the EU, has a major impact on commercially available IVDs (CEIVDs) and…
Read moreEHA Guidelines Workshop series
EHA has initiated a series of online workshops dedicated to guidelines (produced or endorsed by EHA) aimed at disseminating good practices and knowledge for diagnosis and treatment of hematologic diseases.
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