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A Clinical Trial Agreement (CTA) is a legally binding agreement that manages the relationship between the sponsor that may be providing the study drug or device, the financial support and /or proprietary information and the institution that may be providing data and/or results, publication, input into further
A document typically executed by parties intending to collaborate on a sponsored project. The teaming agreement will cover general issues related to intellectual property rights and other aspects defining the reporting and working relationship of the parties..
Contract Tracking System (eCTS): provides the status of incoming agreements handled by the OSP Contracts Unit. Once the CDA is signed by OSP and the sponsor reviews it, you should receive a protocol, contract template, budget (if already prepared, otherwise the Office of Clinical Research (OCR)) will assist.
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.