Watch this Medical Device Development webinar recording to learn more about the quality assurance and testing processes used in the development of medical devices. In such a highly regulated safety-critical industry, software quality, reliability and safety are vital. That’s exactly why risk management, QA and testing, as well as the documentation of these are all regulated in various industry standards (ISO 14971, IEC 62304, and a variety of FDA regulations). This webinar lets you learn more about compliance with these standards, as well as QA and testing processes of medical device software with codeBeamer.

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