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Who Attends

Limit Study Variability • Streamline Data Collection • Ensure Efficient CEC Review • Minimize Regulatory Approval Timelines

May 1-2, 2018
  • Philadelphia, PA

Who Should Attend

You will benefit from attending this event if you are a manager, associate director, director or vice president from a bio/pharmaceutical or medical device company with responsibilities or involvement in the following areas:

  • Adjudication
  • Clinical Operations
  • Clinical Project Management
  • Data Management
  • Medical Affairs
  • Protocol Management
  • Biostatistics
  • Pharmacovigilance
  • Safety

This conference will also benefit consultants,
CROs and technology vendors working with the above audience.

A Great Place to Meet Your Market!

Take advantage of the best opportunity to meet potential clients face-to-face.
Build relationships while demonstrating thought leadership and sharing expertise.
For more information on how to position your company as a sponsor or exhibitor, contact:
John Fosdick at +1-339-298-2142 or email [email protected]

You will benefit from attending this event if you are a manager, associate director, director or vice president from a bio/pharmaceutical or medical device company with responsibilities or involvement in the following areas:

  • Adjudication
  • Clinical Operations
  • Clinical Project Management
  • Data Management
  • Medical Affairs
  • Protocol Management
  • Biostatistics
  • Pharmacovigilance
  • Safety

This conference will also benefit consultants,
CROs and technology vendors working with the above audience.

A Great Place to Meet Your Market!

Take advantage of the best opportunity to meet potential clients face-to-face.
Build relationships while demonstrating thought leadership and sharing expertise.
For more information on how to position your company as a sponsor or exhibitor, contact:
John Fosdick at +1-339-298-2142 or email [email protected]