Die Verordnung (EU) 2017/746 (IVDR) in der Praxis: Umsetzung von Anhang I in der Pathologie

BACKGROUND: Regulation (EU) 2017/746 on in vitro diagnostic medical devices (IVDR) imposes several conditions on pathology institutes that develop and use in-house in vitro diagnostic medical devices (IH-IVDs). However, not all of these conditions need to be implemented immediately after the IVDR en...

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Detalles Bibliográficos
Autores principales: Kahles, Andy, Goldschmid, Hannah, Volckmar, Anna-Lena, Ploeger, Carolin, Kazdal, Daniel, Penzel, Roland, Budczies, Jan, Flechtenmacher, Christa, Gassner, Ulrich M., Brüggemann, Monika, Vogeser, Michael, Schirmacher, Peter, Stenzinger, Albrecht
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Medizin 2023
Materias:
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602947/
https://www.ncbi.nlm.nih.gov/pubmed/37792098
http://dx.doi.org/10.1007/s00292-023-01231-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10602947/
https://www.ncbi.nlm.nih.gov/pubmed/37792098
http://dx.doi.org/10.1007/s00292-023-01231-3

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