The New Gold Standards of IRT Delivery for Clinical Trials

Life Sciences, Clinical Trials, Pharmaceutical, Pharma Manufacturing & Supply Chain,
  • Wednesday, May 03, 2017

Traditional IRT systems manage randomization and drug supplies. This webinar will focus on emerging IRT system functionality that expedites go-live timeline, provides more sponsor control, and full visibility into the whole project lifecycle. The combined impact of these new features offers significantly more efficiencies, cost and time savings and reduced clinical trial risk.

Discussion topics include:

  • Agile development approaches
  • Fully configurable systems and associated benefits
  • New methods of materials management
  • The benefits of unified eclinical management systems


Grant Dietrich, Vice President, Strategic Partnerships, YPrime

Grant Dietrich is Vice President, Strategic Partnerships at YPrime. Bringing 15 years of focused experience in eclinical and interactive response technologies, he provides strategic operational and business development oversight for the company’s key accounts.

Prior to joining YPrime, Grant was Director of Account Management for Cenduit. In his earlier roles, he served as a project manager at ClinPhone, where he designed and managed IRT and ePRO systems.

Following his US Army position as an emergency room nurse, Grant began his industry career as a project manager for Merck and Co. He earned a master’s degree in human relations from the University of Oklahoma and a bachelor’s degree from Rutgers University.

Message Presenter

Who Should Attend?

Managers/Directors/Vice Presidents of:

  • Clinical Operations
  • Clinical Supply
  • Clinical Technology
  • Data Management
  • Procurement/Outsourcing

Xtalks Partner


YPrime offers more than a decade of focused work with eclinical systems to expedite and improve the quality of patient management, clinical supplies, drug accountability and clinical data. Cloud-based interactive response technology (IRT) and electronic clinical outcome assessment (eCOA) platforms offer sponsors greater speed, precision and integration in clinical trial management.

Our data services and tools help sponsors bring together fragmented clinical research data into contextual information they can act on. YPrime’s technology and service offerings enable sponsors to move faster and more efficiently to their next development milestone.

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