Founded in 1989, CPC is recognized for its expertise in comprehensive trial management for both national and international clinical research. CPC is led by Dr. William Hiatt, a specialist in vascular medicine, is a professor of Medicine at the University of Colorado and has extensive experience in the design and management of cardiovascular trials. CPC's Executive Committee has extensive experience in industry, government and academic-sponsored trials. CPC also has considerable regulatory experience, including Dr. Hiatt who recently served as the Cardio-Renal Advisory Committee chairman for the FDA and Dr. Mori Krantz who currently serves on this committee.
Standardizing data collection methods across sites throughout a trial
Controlling variability
Reducing placebo response
This program allows a Sponsor to conduct a more effective trial (less variability translates into more definitive signals, thereby potentially requiring fewer subjects). EQuIP includes site quality programs, which include tailored training videos and reference tools designed to optimize trial conduct. Critical to the success of this program are regular on-site quality interventions with site staff, focusing on their ability to acquire complete and accurate data. CPC's full service management, combined with EQuIP, provides a cost-effective, innovative solution.