Since 1998, Cape Cod Clinical Research, Inc. (CCCRI) has been providing the pharmaceutical and biotech industry, as well as individual study sites, with project management, quality monitoring, GCP auditing, site assessments, and training programs for research personnel.

In addition to corporate headquarters in Hyannis, Massachusetts, CCCRI has established partnerships with a nationwide network of independent consultants. By utilizing this network, CCCRI is capable of providing high quality and efficient consulting while minimizing the strain on research resources.

Our client approach has involved a commitment to understanding and sharing your clinical development goals, while keeping your budgets in mind. We focus our energy and resources on meeting those goals, all the while providing exceptional service.

CCCRI is recognized and respected for providing the following specialized services to clients:

• Clinical Development (Phases I to IV)
  

• Full CRO services
  

• Clinical Study Site Monitoring by nationwide team
  

• GCP Auditing
  

• GCP Training services for both investigative sites and company sponsor
  

• Project Management
  

• Site assessments
  

• Staff Training
  

• Medical Writing
  

• Quality Control Management of Regulatory Documents
  

• TrialDOCS™ -- A proprietary online clinical document management tool
  

• EnrollmentDOCS™ -- A proprietary online Clinical Trial Enrollment Tracker tool