january, 2015

28jan2:00 pm3:00 pmTransforming Clinical Operations with a Fully Integrated eTMF Operating Model

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Event Details

Halloran President and CEO, Laurie Halloran, co-presents a webinar, Transforming Clinical Operations with a Fully Integrated eTMF Operating Model, in partnership with Applied Clinical Trials and Veeva Systems on January 28, 2015.

Transforming Clinical Operations with a Fully Integrated eTMF Operating Model
Learn best practices for development-stage companies looking to transition from a paper-based TMF operating model to a fully-integrated eTMF operating model. Halloran Consulting Group, a global life sciences management consulting firm, has successfully guided clients in all phases of clinical development in leveraging Veeva Vault eTMF to transform their clinical operations with little to no disruption to the flow of normal business operations. See how an eTMF gives these companies greater access, visibility, and control of their clinical studies, allowing them to more efficiently meet study milestones and maintain an inspection-ready TMF. Topics will include deployment strategies, validation best practices, and administration of the eTMF.

PRESENTERS

  • Laurie Halloran, President & CEO, Halloran Consulting Group
  • Bryan Ennis, Director R&D Customer Success, Veeva Systems

Moderated By: Lisa Henderson, Editorial Director, Applied Clinical Trials

YOU WILL LEARN

  • Explain the importance of introducing eTMF technology early in the development cycle
  • Describe the importance of a true multitenant eTMF application for ubiquitous access
  • Understand why a robust and fully defined eTMF process can better help manage risk with fewer resources

WHO SHOULD ATTEND

  • Clinical Development Director and above
  • Document/Records Management Directors
  • Clinical Trial Managers
  • Clinical Data Management/Biostatistics Directors
  • Clinical Monitoring Directors
  • Safety Directors
  • Quality Assurance Directors
  • Clinical Operations Director and above
  • Information Technology Directors
  • Clinical Trial Directors
  • Clinical Trials Materials Director (Tech ops— CMC)
  • Study Start-Up Team Directors
  • Document Control Coordinator
  • Regulatory Operations Directors

Time: 2:00pm EST
Date: January 28, 2015
Place: Online Webinar

For more information and to register, please click here.

Time

(Wednesday) 2:00 pm - 3:00 pm

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