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Validation of medical device software according to MDR

Validation of medical device software according to MDR

by Alexander Fenkiw | Dec 30, 2022 | Unkategorisiert

If you are developing software that qualifies as a medical device under the Medical Device Regulation (MDR), validation is one of the most critical issues. Successful validation of your software is an absolute prerequisite for bringing your medical device to market....

Insider-Empfehlungen für DiGA-Hersteller in 2025
Downloaden Sie jetzt unser Whitepaper

Insider-Empfehlungen für Software-Medizinprodukt-Hersteller in 2025
Downloaden Sie jetzt unser Whitepaper


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kontakt@quickbirdmedical.com
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+49 (0) 89 54998380
kontakt@quickbirdmedical.com

 

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13 wichtige Empfehlungen für angehende DiGA-Hersteller 2025

13 wichtige Empfehlungen für angehende Medizinprodukt-Hersteller 2025

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