FDA issues 2016 planned guidance list

FDA issued “CDRH Fiscal Year 2016 (FY 2016) Proposed Guidance Development and Focused Retrospective Review of Final Guidance” at the link provided.
It includes plans to issue a final guidance on General Wellness Products which is often an intended use for software devices including many Mobile Medical Apps and plans to draft guidances on Medical Device Decision Support Software as well as Medical Device Interoperability.

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IEC 62304 and other Emerging Standards Impacting Medical Device Software

Being Agile & Yet Compliant

ISO 14971 SaMD Risk Management

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Medical Device Cybersecurity

Software Verification

IEC 62366 Usability Process and Documentation

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