Clinical Trial Support

We conduct clinical and pre-clinical studies, as well as providing the following support services through our partner companies:

  • Project management
  • Monitoring
  • External laboratory selection and monitoring
  • Quality Assurance (system, process, qualification, study specific audits)
  • Scientific writing (protocol, report and publications)
  • Data management (EDC/Paper)
  • Medical coding
  • Data capture form (DCF) and electronic case report form (eCRF) design
  • Database design, edit check programming and validation
  • Biostatistics and statistical programming
  • Document management for regulatory submissions
  • Data submissions to regulatory authorities in XML