Government

C-TASC has had the opportunity to serve as a clinical trial resource for a many federally funded projects. Our staff is adept at navigating the project through required regulatory and contractual requirements associated with government funded initiatives.

FDA

C-TASC has proven expertise in converting various formats of clinical data into a FDA-acceptable SDTM format. C-TASC is currently contracted by the FDA to assist in establishing new standard procedures for the receipt, processing and analysis of clinical trial data submitted for FDA approval.

NIH

For two decades, C-TASC staff have collaborated with their counterparts at the clinical sites and the NIH to achieve well run studies, publications, and on-time production of work products. C-TASC coordinates and supports protocol development, power calculations and data analyses for studies funded by the National Heart, Lung, and Blood Institute (NHLBI) and the National Institute of Child Health and Human Development (NICHD).

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