Your investigational product matters to us. See the difference our personalized attention makes when you partner with us to conduct clinical research. With decades of experience in clinical research and hundreds of trials completed by our team, there is no study that is too big, small, or complicated for us to handle.
We offer cover-to-cover solutions from the design of the study, development and approval of protocols, submission of investigational new drug (IND) or investigational device exemption (IDE) to the FDA, monitoring, conducting the clinical study in our own facilities, and identifying the best sites at our partner organizations to ensure timely recruitment of patients.
Our unique, team-based structure is designed to improve outcomes, maximize efficiency, and decrease timelines for our stakeholders. On-site imaging technologies, including ultrasound, CT scans, and digital X-rays, plus in-house laboratory and pharmaceutical services allow us to meet complex monitoring, storage, or compounding requirements. Our combined decades of experience building dozens of protocols, building research networks, and managing hundreds of clinical trials is rare to find in a company of this size.
Let us discuss how we can work together to accomplish your goals and provide personalized attention for your investigational product. Our team utilizes a hands-on approach to every clinical trial, explore how that can make a difference for you.
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