Simplifying the Clinical Trial Regulatory Submission Process

The convergence of technologies in the clinical trials space is improving efficiencies on all fronts of the clinical research process. Direct work with a focus group composed of representatives from many walks of the industry have led our group to the conclusion that a source of difficulty largely unmitigated by available technologies today is the regulatory document tracking and submission process.

Under the guidance of this group this webinar will explore the ways in which a unified Clinical Trial Management System (CTMS) can deliver efficiencies across an enterprise of clinical development. Pulling the regulatory submission process into a software platform that has truly unfettered access to its data allows for powerful reporting, elimination of redundant tasks, and the reduction of risk due to human error.

The advantages of a single unified source of clinical operations data become easily apparent when viewed through the lens of a modern Clinical Trial Management System and the emerging paradigm for clinical trial technologies as a whole.

Speaker

Patrick Smith, Technical Marketing Writer, DATATRAK

Patrick Smith graduated from Texas A&M with a Bachelor of Science in Computer Science and a Bachelor of Arts in International Studies. He joined DATATRAK in 2012 as a Technology Associate aiding in technical writing and market research. Patrick quickly began to shine and was promoted to Technical Marketing Engineer in June 2013. In this role he provides marketing content, compiles market and competitor research, conducts product demos, and works with Product Management in the design, testing, and documentation of DATATRAK ONE UX™.

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