Learn how top pharmas and CROs plan to speed database build and data collection, as well as their top challenges and future priorities. From this webinar you'll gain insights into:

  • Taking an agile approach to database build
  • Reducing UAT timelines with a risk-based approach
  • Driving innovation at your organization
This in-depth research from Tufts follows their industry-wide eClinical Landscape Study, examining the major cause of database build delays and their impact on trial cycle times.

Featured Speakers

Ken Getz

Director of Sponsored Programs
Tufts CSDD

Ken Getz is an internationally recognized expert on pharmaceutical R&D management, protocol design, outsourcing, data management, investigative site management and patient engagement.  Mr. Getz has published extensively in peer-review journals, books, and in the trade press. Ken is also the founder of CenterWatch, a leading publisher in the clinical trials industry.

Richard Young

Vice President, Vault EDC
Veeva Systems

With almost 25 years of experience in life sciences, Richard is known for his executive vision and proven operational experience in data management, eClinical solutions, and advanced clinical strategies. Most recently, Richard served as vice president of global consulting partners at Medidata Solutions, consulting on adaptive trials, risk based monitoring, big data, mobile health, and other major data strategies with sponsors and partner organizations across the globe.

NOW AVAILABLE ON-DEMAND

Register now for this webinar