Harrison Clinical Research | Harrisonclinical - clinical operations phase ii iv
Harrison Clinical Research
In all our offices, clinical operations teams offer a wide network of monitors, both locally and centralised, and can conduct and manage all or parts of your clinical studies from Phase II-IV, with regard to design, management, monitoring and reporting. All our studies are carried out to the standards of ICH-GCP and all procedures and data collected are audited and subjected to our in-house Quality Assurance. Our staffs all have medical/scientific backgrounds and undergo continual, documented training. Each CRA only monitors a limited number of studies and/or sites, to enable them to maintain the level of attention your project requires. Your project manager will offer you solutions rather than questions and will report back directly to you, ensuring project continuity and good relationships between CRAs, site personnel and the sponsor, whilst managing your study on time and within budget.
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