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Proven Technologies & Best Practices Taken a Step Further

With years of valuable experience supporting clinical studies, our teams of PhD and MS biostatisticians are up-to-date and fluent in emerging software technologies, ensuring that when tomorrow arrives, we’ll be ready and waiting.

Collectively, we offer unmatched expertise in monitoring, statistical design/analysis, and SDTM conversion.

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Related News

FDA Selects C-TASC for Statistical Analysis Support and SDTM Clinical Data Conversion.

Baltimore, Md. – November 2, 2009 – Clinical Trials & Surveys Corp. (C-TASC), a clinical trials solutions company, announced today it has received four new task orders ...

Related Projects

Task Two: SAS Programming Support for the Investigation of Adverse Events Reported in Association with Influenza Therapy..

SAS Programming support  for  this ongoing FDA investigation  to analyze the largest US database of adverse drug events to further characterize adverse ...

Task Seven: MAED Service Enhancements..

MAED Service is a server-based adverse event analysis tool which enables reviewers to quickly generate a large number of adverse event analyses in a batched manner. The ...

Task One: Data Management and Statistical Programming to support Center for Drug Evaluation and Research (CDER) reviewers.

Basic Data Center activities included providing data management, statistical and research leadership to support the FDA in analyses of current NDAs and conversion of ...