How Data Aggregation and Visualization Transforms Clinical Trials

posted on 4th December 2013 in Recommendations

There are intense pressures on clinical trial sponsors to change the way clinical research is conducted in order to decrease costs and speed up the research and development process. There is also increased scrutiny by regulatory agencies such as the Food and Drug Administration and European Medicines Agency, and compliance with regulations is critical. The ultimate […]

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Is Your Clinical Trial Data Efficiently Integrated?

posted on 3rd December 2013 in Solutions

Life sciences companies are drowning in data! It is a challenge for life science companies to know what data they have, and it is nearly impossible for them to look at their clinical trial data holistically and act on it. Technology continues to evolve and is dramatically changing how clinical trials are conducted. In particular, […]

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Leverage Technology For Data Aggregation from Disparate Sources

posted on 14th November 2013 in Solutions

Sponsors are facing intense pressures to change the way clinical research is conducted in order to decrease costs and speed up the research and development process. Equally important data management challenges are: 1) The ability to enhance data sharing between partners such as study sites, CROs, clinical trial monitors, and development partners such as small or […]

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Join The eClinical Solutions Conversation!

posted on 11th November 2013 in News & Events

Welcome to the eClinical Solutions blog! Our team of clinical development and programming professionals are passionate about how technology can accelerate clinical data management. Our mission is to maximize insights into your clinical trial data. Topics we’ll focus on include: Advances in clinical trials such as moving trials to the cloud and risk-based data monitoring […]

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Transforming Clinical Trials: The Ability to Aggregate Data Efficiently and Make Impactful Decisions

posted on 11th November 2013 in White Papers

Clinical trial sponsors are facing intense pressures to change the way clinical research is conducted in order to decrease costs and speed up the R&D process. There is also increased scrutiny by regulatory agencies such as the Food and Drug Administration and European Medicines Agency, and compliance with regulations is critical. The ultimate goal is […]

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