Bridging Regulatory Quality and Operational Efficiency with Open Standards

Save your seat for the upcoming webinar!
Accelerating clinical trials with open standards
Central to the elimination of bottlenecks and unnecessary rework in the clinical trial continuum is automation and integration between eClinical applications based on open standards.
Existing systems (CTMS, eTMF, etc.) only support clinical trial functions in silos. The challenges in integration of eClinical systems stems from the lack of standards, it’s simply not enough to have APIs available.
Standards provide stakeholders with a basis for mutual understanding and are critical tools to facilitate communications. Open standards help fuel compatibility, interoperability, simplify trial executions and speed time-to-market.
The new eTMF Exchange Mechanism provides the cornerstone in collaboration between all study startup and executive stakeholders, including sponsors, CROs, investigative sites and regulatory and ethical committees.
Date/Time:  August 28, 2018 @ 3:00 pm BST, 10 am ET, 7 am PT
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Author: rammellel

Records management consultant to the life sciences / pharmaceutical industry

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