How does the notified body assess your clinical evaluation?
February 18, 2021How to perform a clinical evaluation for Medical Device Software
January 28, 2021How to ensure sufficient clinical evidence for legacy devices
January 15, 2021How to claim an equivalence in the clinical evaluation under the MDR
December 21, 2020
Novelties for Clinical Evaluation and Post Market Surveillance within MDR – the Posts Series
December 10, 2020
Bei Medizinprodukten auf die EU warten hilft der Schweiz wenig
December 3, 2020
Revision der Schweizer Medizinprodukteverordnung mit Folgen
August 14, 2020
Interpellation Jacqueline de Quattro on medical devices
June 2, 2020
Politics intervene regarding medical devices
May 8, 2020
EU MDR audit requirements and links to MDSAP program
February 14, 2019
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