Our Southern California sites feature the following:

• Medical and research staff that are employees of CCT, so that CCT is not an SMO (Site Management Organization)
• Standardized regulatory filing including centralized IRB submission and documents
• Quality Assurance programs to insure consistency across sites. Enhanced reliability in data collection and rating scales tied to ongoing multi-site training programs
• Implementation of patient education about placebos, demonstrated to improve the separation between placebo and active treatment
• Simplicity for the Sponsor and CRO in managing the flow of information, scheduling site visits, etc.
• Depth to cover all patients in clinical studies, allowing enrollment to proceed as promised, irrespective of staff turn over (which is low), vacations, and sick leave