Clinical Trial Delivery

Our multidisciplinary team approach includes Academic Scientific Leadership alongside Clinical Trial Delivery ensuring our trials are conducted to rigorous quality standards. You can expect to work with a competent and efficient team at all stages of project development both pre and post funding award.

We can provide:
  • Funder / funding advice
  • Statistical design and sample size calculations
  • Grant proposal development and peer review
  • Study protocol writing
  • Development of patient information leaflets
  • Design of case report forms and questionnaires
  • Ethics submissions and regulatory approvals
  • Information Systems design and management
  • 24-hour automated randomisation service
  • Customised GCP-compliant database build (with option for electronic remote data capture systems)
  • Integrated data validation
  • Trial management and coordination
  • Trial monitoring (central and on-site)
  • Trial financial planning and costings
  • Linkage with health economic, qualitative and quality of life researchers and development and design of linked evaluations
  • Research governance and compliance with regulatory requirements
  • Analysis and reporting