BOSTON & GENEVA--(BUSINESS WIRE)--eTMF Optimize from PHT Corporation supports faster new drug submissions and improves clinical trial execution with rapid, regular population of the electronic trial master file (eTMF). PHT is the leading provider of technologies used to collect patient-driven eData for clinical research.
The TMF is a collection of essential documents used by a trial sponsor to record how they fulfilled their clinical trial obligations. These documents demonstrate investigator, sponsor and monitor compliance with regulatory requirements including FDA 21 CFR 312.50 and EU No. 536/2014, Article 57.
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The TMF is a collection of essential documents used by a trial sponsor to record how they fulfilled their clinical trial obligations. These documents demonstrate investigator, sponsor and monitor compliance with regulatory requirements including FDA 21 CFR 312.50 and EU No. 536/2014, Article 57.
Help employers find you! Check out all the jobs and post your resume.
