Global Compliance

Market Application and Lifecycle Management: The Road to Commercial Success

TORONTO (PRWEB) APRIL 30, 2021 — Preparing your market application and planning the lifecycle management of your development program is critical to moving your product through early-phase trials and achieving commercial success. Approval in the United States and European Union paves the way for a drug’s acceptance in many, but not all, other parts of the world — so which additional countries should you consider incorporating in your clinical trial strategy?

Register for this webinar to explore these and other product development subjects. We’ll also explore case studies from recent product approvals. Topics will include:

  • The importance of developing a risk evaluation mitigation strategy, especially if risk factors require limited product distribution
  • Making post-approval product changes, such as switching manufacturers
  • The expanding role of pharmacovigilance in identifying potential safety issues

Join expert speakers from Premier Research, Kristi Miller, Ph.D., Vice President, Regulatory Affairs, Regulatory Professionals; Christopher Hendry, Senior Director, Technical Services, Regulatory Professionals; and Lee McGuinness, Executive Director & Global Head of Pharmacovigilance and Medical Device Vigilance, in a live webinar on Wednesday, May 19, 2021 at 11am EDT (4pm BST/UK).

For more information, or to register for this event, visit Market Application and Life-Cycle Management: The Road to Commercial Success.