Clinical trials typically generate a significant volume of documentation. With distributed teams and many organizations involved in the conduct of trials, centralizing and organizing content in one place can be challenging. Ensuring that all team members have access to trial information at all times and allowing them to collaborate together is a key ingredient in the new clinical trial organization. Regulators are also providing more clarity in terms of their expectations regarding records and eTMF, so ensuring timely collation of records and enabling content to be easily searched and understood is now a requirement.
This session will discuss these trends and how technology can support and empower organizations to work within this new paradigm. We will cover the following topics:
Overview of new organization models in clinical R&D
Cloud based document collaboration
Centralized content repositories
Centralizing regulatory submissions
Leveraging content to produce metrics and reporting
Webinar´s time (GMT -5:00) Eastern Time (US & Canada), Bogota, Lima
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