The De Novo Process and the FDA’s Final Rule to Simplify Medical Device Classification Procedures

The De Novo process is a complex process that has significant implications for the manufacturer of post-amendment devices in terms of how their devices are classified. In addition, the FDA has recently revised the regulations in 21 CFR part 860 that pertain to the reclassification of devices in this category. This webinar will be essential in your continued understanding of this process and in your compliance with the new regulation changes.

For devices that are innovative, when a predicate is found not to exist, The De Novo classification process, also known as “Evaluation of Automatic Class III Designation,” is a device classification process that provides a pathway to either a Class I or Class II classification for medical devices for which general controls or general and special controls provide a reasonable assurance of safety and effectiveness, but for which there is no legally marketed predicate device.

This webinar will review this De Novo process in conjunction with the recent changes to 21 CFR 860 that pertain to the reclassification of these post-amendment devices and the De Novo process in general.

Areas Covered in the Session :

  • The De Novo Classification Process
  • When the De Novo Process may be used
  • Submitting a De Novo Request for FDA Review
  • Review Process for De Novo Requests
  • 21 CFR 860 regulation changes as they relate to the De Novo process
Who Should Attend:

  • Regulatory Departments
  • Manufacturing Departments
  • Compliance Departments
  • Documentation Departments
  • Training Departments

MD2963

Charles Paul

Charles Paul is an instructional designer and management consultant with over 30 years’ experience providing training and consulting services to regulated industries. He has installed quality systems and designed and developed GMP and operational documentation and training programs for foods and beverage, pharmaceuticals, biotech, cosmetics, and consumer product – OTC industries.

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  • 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
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