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Clinical trials can include an independent, unbiased adjudication committee to evaluate the impact of clinical events on the overall study....

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To reduce the development time and risk of rework inherent to most IRT systems, we’ve developed a robust core system...

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The Bioclinica EDC Solo delivery model combines the full features and functionality of Bioclinica EDC, which is used by Bioclinica’s...

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Accelerate database lock and gain confidence in the data for your regulatory submissions with full-service Clinical Data Management (CDM) that...

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A Clinical Trial Management System (CTMS) is used to centralize data and automate processes for better decision making. Typically, an...

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The clinical supply chain represents a particular need in clinical trials to synchronize many complex processes and multiple organizations. Without...

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As of May 5, 2017, the US Food and Drug Administration is only accepting submissions in Electronic Common Technical Document...