Services - Clinical Research

Our experienced team of clinical research professionals has recent / current experience of the following projects:

• Clinical project management
  • Supporting clients in the management of studies conducted by other CROs
  • Providing expert clinical research input to product development teams
• Clinical study monitoring
  • Phase II study - UK sites - treatment for side effects of chemotherapy in Cancer patients
  • Phase I study - UK - Oncology patients
  • Phase I study - USA - Oncology patients
  • Phase I studies in healthy volunteers - UK - several
  • Phase I study in renal impairment substances
  • Phase I studies in treatments for addictions
  • Phase I study in patients with MS
• Clinical protocol writing
• REC and GTAC submissions - UK
• Clinical study report writing / publication preparation
• Investigator Brochure preparation and annual update
• Unblinded safety reporting coordination

Clinical Research Summary

• Clinical Programme Strategy and Management
• Protocol Development
• Clinical Investigator identification
• Phase I unit selection and systems audit
• GCP monitoring - Phase I
• Phase II clinical study management and monitoring
• Statistics and data management
• Medical writing
• QA audit
• Investigator meeting organisation
• Laboratory selection
• Drug manufacturer selection