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Monthly Medical Device Webinar - Combination Products: Navigating Complex Pre- and Post-market Requirements

Date: Wednesday, February 27, 2019 12:00 PM - 1:00 PM

Combination products present a number of regulatory and strategic challenges around both premarket pathways and postmarket compliance. This seminar will provide:

  • an overview of the definition of combination products
  • how to determine the appropriate premarket review pathway
  • compliance with postmarket requirements, and
  • strategies for interacting with FDA.

The webinar will be led by Kristin Davenport and Christina Kuhn.

To RSVP click here.

Log-in details will be distributed to registrants closer to the date of the webinar.