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Who Should Listen:  Medical device developers, trial sponsors, clinicians, R&D, site management personnel, and regulatory personnel looking to better understand the current research trends in global cardiovascular device development.

What You'll Learn:  Join our panel of industry experts for this interactive presentation to learn five easy steps to help ensure the success of your global cardiovascular medical device trial:

  • Selecting study sites, emerging vs. mature venues
  • Streamlining variations in global regulatory requirements, including increased safety requirements and better-defined study endpoints
  • Moving to eClinical platform with access to real-time data and risk-based monitoring
  • Maintaining consistent global standards of care
  • Implementing operational considerations (i.e., clinical supply management and supply chain infrastructure)


  • Carol Duffy, D.O., FACC
    Executive Medical Director, Clinipace Worldwide
  • Rick Cutcher
    Senior Director Project Management, Clinipace Worldwide
  • Debbie Rosenfelder
    Clinical Trials Manager, Clinipace Worldwide

Free Webcast:

5 Steps to Success for Your Cardiovascular Medical Device Trial

Watch the webcast today!