FDA CDRH Standards Recognition Guidance

FDA issued “Recognition and Use of Consensus Standards; Final Guidancefor Industry and FDA” which supersedes the February 19, 1998 guidance. It describes the general requirements for use of FDA recognized standards in premarket submissions. It indicates that new inspection policy will include inspection of evidence of conformance to any standards for which conformance is claimed in submissions. The full guidance is at the link provided.

SoftwareCPR Training Courses:

IEC 62304 and other Emerging Standards Impacting Medical Device Software

Being Agile & Yet Compliant

ISO 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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