FDA Basic Intro Quality System Regulation

The presentation “Quality System Regulation 21 CFR 820 Basic Introduction” by Kimberly A. Trautman CDRH Medical Device Qualtiy System Expert at FDA is a brief overview of this central regulation for medical device manufacturers with some extra emphasis on Design Control elements. The full presentation is at the link provided.

SoftwareCPR Training Courses

ISO13485:2016 ISO 13485 Internal Audit(or) Training Course (Live, 3-day)

IEC 62304 and other Emerging Standards Impacting Medical Device Software (Live, 3-day)

Being Agile & Yet CompliantISO 14971 SaMD Risk Management

Software Risk Management

Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

Or just email training@softwarecpr.com for more info.

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