Cargando…
Laboratory-Developed Tests: Design of a Regulatory Strategy in Compliance with the International State-of-the-Art and the Regulation (EU) 2017/746 (EU IVDR [In Vitro Diagnostic Medical Device Regulation])
PURPOSE: This study aimed at the development of a regulatory strategy for compliance of laboratory-developed tests (LDTs) with requirements of the Regulation (EU) 2017/746 (“EU-IVDR”) under consideration of international requirements for LDTs as established in major regulatory regions. Furthermore,...
Autores principales: | Spitzenberger, Folker, Patel, Jaimin, Gebuhr, Inga, Kruttwig, Klaus, Safi, Abdulrahim, Meisel, Christian |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8294224/ https://www.ncbi.nlm.nih.gov/pubmed/34291407 http://dx.doi.org/10.1007/s43441-021-00323-7 |
Ejemplares similares
-
Die Verordnung (EU) 2017/746 (IVDR) in der Praxis: Umsetzung von Anhang I in der Pathologie
por: Kahles, Andy, et al.
Publicado: (2023) -
The importance of regulation (EU) 2017/746 for quality control in medical laboratories
por: Ialongo, Cristiano, et al.
Publicado: (2021) -
Advisory opinion of the AWMF Ad hoc Commission In-vitro Diagnostic Medical Devices regarding in-vitro diagnostic medical devices manufactured and used only within health institutions established in the Union according to Regulation (EU) 2017/746 (IVDR)
por: Hoffmüller, Petra, et al.
Publicado: (2021) -
Structure and content of the EU-IVDR: Current status and implications for pathology
por: Kahles, Andy, et al.
Publicado: (2023) -
Experience With IVDR Implementation in Three Diagnostic Laboratories: Messages to EU Health Institutions, Diagnostic Healthcare Payers, and Authorities
por: Lubbers, Bart R., et al.
Publicado: (2023)