Is Your Medical Device Software 510k Ready?

One of the main reasons that submitting a 510K for Software Enabled Medical Devices or Software as a Medical Device can fail to get approval by the FDA is due to deficient or missing documentation. This Seminar will describe what is the FDA is expecting in the 510K submittal and how to make sure that the documentation meets those expectations.

Why You Should Attend:

This course will ensure that Device companies will know exactly what documentation needs to be prepared. They will also know how to ensure the documentation is prepared correctly specifically for the software portion of the submittal so that it will be in compliance preventing delays of the 510K approval.

Companies can also face potential audit risks and serious findings post submittal that can block their ability to ultimately sell their product successfully. This course will ensure that you know what is expected to have in place for compliance for your company during the preparation of a 510K to prevent this risk.

Areas Covered in the Session :

  • Know exactly what software documentation needs to be prepared for a Class II/B/Moderate Level of Concern for the Software Portion.
  • Know how to ensure the software documentation is prepared correctly specifically for the software portion of the submittal so that it will be in compliance preventing delays of the 510K approval.
  • Avoid potential audit risks and serious findings post submittal that can block their ability to ultimately sell their product successfully.
  • Know what is expected to have in place for compliance for your company during the preparation of a 510K to prevent this risk.
  • Ensure a faster 510K approval because the documentation is complete and comprehensive.
  • Prevent costly time to market issues because 510K has been rejected completely because of software.

Who Should Attend:

  • Medical Device Software Regulatory professionals,
  • Medical Device Software Quality Assurance Engineers,
  • Medical Device Software Quality Senior Management,
  • Medical Device Software Company Senior Management
  • Medical Device Quality Engineers
  • Medical Device Quality Senior Management

MD2843

Nancy Knettell

Nancy Knettell, Founder and Principal at Software510K, LLC, has over 30 years in combined mechanical design, software development, and systems engineering experience primarily in the medical device industry as a Software Verification, Validation/Systems Engineer.

Along with her senior level management experience with cross-functional program teams for major companies such as EMC and United Technologies, Nancy has also consulted to major medical companies such as Smith and Nephew, Philips Medical, CR Bard, Kollsman Medical, Applied Biosystems, Deka Research, Avedro and Hologic.

But, for Nancy, involvement in medical device development is a personal issue. Having lost her father at an early age to heart disease, she now wants to work to help other people facing such life threatening events. It is her mission to advance the potential for life-saving medical devices through the use of quality based engineering systems.

Refund Policy

membership
  Go PRIME   🛈 $ 240 SELECT
  Personal Plan 🛈 $ 3000 SELECT
  Business Plan 🛈 $ 9000 SELECT
  • Login Information with Password to join the session, 24 hours prior to the webinar
  • Presentation Handout in .pdf format
  • Presentation from the Speaker
  • Feedback form
  • Certificate of Attendance
  • Recording access Information with Password to view the webinar, will be sent 24 hours after the completion of the Live webinar.
  • Presentation Handout in .pdf format
  • Certificate of Attendance