Technical support, resources, tips, and answers to frequently asked questions regarding the CITI Program.

Recently Added CTA Modules

Expand your organization's Human Subjects Research (HSR) education offerings with CITI Program's newest CTA modules.  These modules can also be used in CRC Foundations, Good Clinical Practice (GCP), and Essentials of Research Administration courses.

Clinical Trial Agreement (CTA)

CTAs are one of several key documents that govern the conduct of clinical trials. They serve as a legally binding contract between a sponsor, site, and researcher, and outline each party's responsibilities and obligations for the clinical trial. It is imperative that researchers and sites understand the importance of CTA development, negotiation, and execution, as effectiveness in these areas will increase efficiency, protect researchers/sites and subjects, and help advance research. To help meet these needs, four new modules are available from CITI Program: 

  • Overview of the CTA
  • Understanding the Terms of the CTA
  • Role of the Researcher and Site in Managing the CTA
  • CTA Negotiation for Researchers and Sites

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Last Updated: 07-Dec-2017 10:18 a.m. EST

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