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Clinical Research Contracts Administration
The Clinical Research Contracts Administration Office is responsible for the negotiation and execution of industry-sponsored clinical trial agreements (CTAs).
Clinical trial agreements handled by the CRCA team have the following characteristics:
- They involve human subjects or human subject records and require Institutional Review Board review or exemption.
- They are funded, directly or indirectly, by a for-profit entity.
Submit your requests for CTAs in eSIFTER.
CRCA is also responsible for the negotiation and execution of Confidential Disclosure Agreements (CDAs), also known as Non-Disclosure Agreements (NDAs), preceding human subjects research, such as those for review of a clinical trial protocol.
Research teams can submit CDA requests through the Clinical Trial CDA intake form.