Implementing a Scalable eTMF Model for Faster Clinical Trials and Drug Launches

Clinical records need to be produced in a timely manner for inspections and audits, but for many life sciences, medical devices, and research organizations, meeting such requirements is a difficult and time consuming task. Due to the collaborative nature of producing requirement documents, organizations need an end-to-end operational model that leverages an efficient document management system and a centralized team to coordinate with internal and external stakeholders.

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