Phase II-IV Clinical Drug Development

With the power of four sites and the simplicity of one company, CCT delivers efficiency and convenience for Sponsors. We offer consistent results and outstanding performance in all of our Phase II-IV services.

Our four 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

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