CCCP Services print

CCCP provides with the following services to pharmaceutical and biotechnology companies for their Phase II, III and IV, bioequivalence and pharmacokinetics studies:

  • Protocol and other essential study document design and development
  • Feasibility studies
  • Regulatory and IRB approvals for clinical trials
  • IMP import and sample export approvals
  • Translations of study documents to and from English
  • Site and Investigator identification and selection
  • Central laboratory identification, selection and liaison
  • Investigator meeting arrangement
  • Site initiation
  • Site monitoring and management
  • Co-monitoring
  • Site closure
  • Project management
  • Logistical support for all imports and exports
  • Medical Monitoring
  • Drug Safety Monitoring
  • Data management
  • Statistical analysis
  • Final reports
  • Archiving
  • Quality assurance
  • Site and study audits

CCCP’s clients always have the option to outsource the whole project to us or select only those services that they need. Moreover, our clients can opt for in sourcing needed personnel on a short-term and/or long-term basis.