One of the most critical factors in the success of a clinical trial is the selection and proper management of qualified investigational sites. Aris can assist you in choosing sites that have the appropriate patient population and possess the necessary facilities to participate in your trial. Our practice of creating a study-specific pre-qualification process allows for a far more accurate selection of appropriate investigational sites.
Our broad therapeutic experience and network of regional CRAs enables us to quickly and comprehensively evaluate sites to determine their suitability for your project. We ensure that sites have access to eligible patients and that their facilities, equipment, and staff are adequately suited to meet your protocol requirements. Our regular communications with site personnel ensure that most problems are identified and resolved proactively — resulting in a measurable value to your study timeline.
