Clinical Services Feasibility


Due to CTI’s therapeutic focus, our team has existing relationships with many Academic Medical Centers (AMCs) and hospital-based research centers around the world. Pre-existing relationships result in expedited study start-up, including regulatory tasks (i.e. International Review Board [IRB]/Ethics Committee [EC] approvals), contracting, and site initiations. Our Legal team has numerous years of international Clinical Trial Agreement (CTA) negotiating experience. We routinely assist in site selection, picking sites that have the highest likelihood of recruiting the necessary patients, with the help of our large internal database of potential investigators/sites in our focused therapeutic areas around the world. When we manage study start-up, the total start-up time is generally less than half the industry average.

Shawna Bredek
Director, Clinical Project Management
With nearly 20 years of industry and clinical experience, including site monitoring and trial management, Shawna has proven her ability to effectively lead complicated clinical trials, including many in pediatrics. She leads the North American Feasibility team, in addition to managing multiple global trials.

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CTI offers the following benefits to site selection:

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