Services: Clinical Trials
Cato Research provides comprehensive and quality Phase 1 through Phase 4 clinical trial services in multiple therapeutic areas.
Our clinical study teams have broad therapeutic backgrounds and clinical experience in related fields (e.g., nursing, laboratory and medical technology, biology, etc.), and have extensive experience in monitoring and managing clinical trials in various therapeutic areas and types of products (drugs, devices, and biologics).
Clinical Trial Management
Cato Research designs, manages, and conducts Phase 1 through Phase 4 clinical studies, ever mindful that quality, time, and cost are critical to sponsors. Our approach focuses on effective, mutual communication, partnership, and flexibility in developing strategies with your specific needs in mind. Our experienced project teams create individualized strategies, and support this work with advanced protocol and case report form development to keep the project on track. We can completely manage your clinical development program or integrate with your staff as a true extension of your company. By partnering with Cato Research, you can ensure that your clinical trial gets the attention it deserves.
Our team of medical and scientific professionals is able to identify potential investigators and maintains a database of investigational sites. We also provide effective strategies for rapid patient recruitment. We can design, manage, and conduct comprehensive investigator meetings for multiple-site studies. We have highly proficient monitoring staff experienced in conducting site evaluation visits, site initiation visits, periodic monitoring visits, and study termination visits as well as all in-house monitoring functions, including adverse events reporting, and clinical trial material management.
Our monitors are all well acquainted with the needs of our clinical data management group, enhancing the efficacy of the entire process. All clinical monitoring activities are performed according to established ICH guidelines to ensure compliance with cGCPs.
Our international network of full-time CRAs offers the benefits of reduced travel time and expense as well as efficient access to sites for monitoring. Our staff speaks more than 13 different languages which enables us to monitor and manage sites across the globe and to provide effective communication and strong support to maximize success.