How to Shorten Study Start-Up by Bringing eTMF into the
The processes of collecting, reviewing and approving clinical documentation (such as CVs, ethics committee approvals, case report forms, informed consents and so forth) during study startup can be a burdensome task for clinical research teams. Find out how Veeva Systems and Medidata Solutions are addressing this need as they discuss how the seamless flow of documents and metadata between Vault eTMF—Veeva’s electronic trial master file (eTMF) application—and the Medidata Clinical Cloud turn the traditional eTMF from an electronic storage drive into a key component for study execution.
Join us for this complimentary webinar to better understand the benefits of dynamically managing documents throughout the study lifecycle by:
- Removing redundant steps from traditional processes, and
- Improving document quality with seamless access to documents
by all users and a clear audit trail.
|Who Should Attend:||Clin Ops, Clinical Research, Portfolio Management, Regulatory Affairs|
|Date:||Thursday, March 7, 2013|
|Times:||10:00 a.m.–11:00 a.m. ET / 15:00–16:00 UK Time
2:00 p.m.–3:00 p.m. ET / 19:00–20:00 UK Time