Non-Clinical Phase
Non-Clinical PhaseNon-Clinical Phase

C-TASC staff follow the ICH M3(R2) guidelines for developing your company’s non-clinical materials. This covers GMP and GLP evaluations and animal studies to evaluate the pharmacokinetics and pharmacodynamics of potential treatments.

Phase I-II
Phase I-IIPhase I-II

Phase I and Phase II studies are generally small in nature (14 to 50 patients) and will give the investigators key information about the future utility of their treatment.

Phase III-IV
Phase III-IVPhase III-IV

The Phase III trial is the pivotal study used by FDA staff to determine if the pharmaceutical/biologic under investigation should be licensed for sale to the population. The Phase IV trial is designed to collect additional material on efficacy and adverse events, after the NDA submission.

SDTM Data Conversion
SDTM Data ConversionSDTM Data Conversion

C-TASC has proven expertise in converting clinical data into an FDA-acceptable SDTM format. C-TASC has developed an automated, high-speed process to convert data for more than 60 FDA studies in 2009 alone.

Consulting/CRO Activities
Consulting/CRO ActivitiesConsulting/CRO Activities

Working as a seamless extension of your business, C-TASC provides all required contract research organization (CRO) services to government, university and private clients.

Discover one of America’s most accomplished clinical research resources. Clinical Trials & Surveys Corp. (C-TASC) offers over 20 years of best practices for the most efficient completion of clinical trials and studies.Discover one of America’s most accomplished clinical research resources. Clinical Trials & Surveys Corp. (C-TASC) offers over 20 years of best practices for the most efficient completion of clinical trials and studies.
(C-TASC) is an employee owned company that offers statistical planning and analyses, data management, medical monitoring and clinical coordination services to governmental entities, non-profit organizations and commercial businesses. Accordingly, we support any or every phase of your process with proven expertise to help you achieve the accuracy, efficiency and scientific integrity you demand. Let us assist you in designing, conducting, and reporting on any clinical trial or clinical development process you are interested in!(C-TASC) is an employee owned company that offers statistical planning and analyses, data management, medical monitoring and clinical coordination services to governmental entities, non-profit organizations and commercial businesses. Accordingly, we support any or every phase of your process with proven expertise to help you achieve the accuracy, efficiency and scientific integrity you demand. Let us assist you in designing, conducting, and reporting on any clinical trial or clinical development process you are interested in!
  • Government

    C-TASC staff has served a variety of government agencies as a clinical trials solutions company, earning the confidence of a variety of notable institutions such as the Food and Drug Administration (FDA) and National Institutes of Health (NIH).

  • Consulting

    C-TASC consulting services bring decades of hands-on experience and offer unmatched expertise in statistical consulting, regulatory advice, monitoring services, biorepository management, and data management services to support the full spectrum of clinical trials.

  • Technology

    Proven technologies and best practices are taken a step further. C-TASC is a fully functional software development organization. Utilizing leading-edge software and design, combined with intellectual capital and experience, C-TASC software has provided Web-based data management solutions for large and small studies.