QuickBird Medical
  • Case Studies
    • Case Studies
    • Customers
  • Services
    • Development: DiGA
    • Development: Medical Software
    • Development: Health Apps
    • Development: Decision Support Systems
    • Development: Wearables for Medical Devices
    • Legal Manufacturer for Medical Devices
    • BSI TR-03161 for DiGA
    • Support for your Software Team
    • Further Services
  • Insights
  • About us
    • Team
    • Jobs
  • Contact
  • German
Select Page
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


Sie planen eine Medical Software oder DiGA?

Sprechen Sie mit unserem Geschäftsführer Malte Bucksch

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

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

 

Whitepaper

13 important recommendations for DiGA manufacturers in 2025

13 important recommendations for medical device manufacturers in 2025

Current

DiGA and Medical Software News

Digital Health Events 2025

Press – QuickBird in the media

© 2025 Imprint | Data protection