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Patientensicherheit durch Qualitätssicherung in der In-vitro-Diagnostik – Webinar 2024 der Ad-hoc-Kommission In-vitro-Diagnostik der Arbeitsgemeinschaft der Wissenschaftlichen Medizinischen Fachgesellschaften (AWMF)

2025/07/11 by Michael Vogeser, Monika Brüggemann, Vogeser, Michael +8
Economics, Econometrics and Finance · Medicine · #Clinical practice guidelines implementation #Health Systems, Economic Evaluations, Quality of Life #Medical and Health Sciences Research #Medicine and health

paper · doi:10.3205/000341

openalex publication_date 2025/07/11 · openalex created_date 2025/10/10 · openalex updated_date 2026/08/01

Abstract

The reliability of laboratory tests is ensured in particular by the interaction of regulated market access and certification of diagnostics, scientific evidence through guidelines, the guideline of the German Medical Association on quality assurance of laboratory medical examinations mentioned in § 9 of the German Medizinproduktebetreiberverordnung, as well as standardisation and accreditation. The Webinar 2024 of the Association of Scientific Medical Societies in Germany's (AWMF) Ad-hoc Commission on In-vitro Diagnostics on 9 October 2024 highlighted this thematic network in four presentations from the perspective of the Federal Ministry of Health, the AWMF Institute for Medical Knowledge Management (IMWi), the German Accreditation Body (DAkkS) and the German Medical Association.

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