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The Clinical element of drug development encompasses all aspects of the clinical trials process; from first in human studies through submission and drug/device approval (phases 1-4). Experts working in this space usually specialize in certain therapeutic areas, as the study design in some spaces differs to others. There are many individuals involved in the various drug/device development phases, to include Biostatisticians, Medical Directors and Data Managers.
Our specialism breakdown includes:
Clinical Trial Managers
Regulatory Medical Writing
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