Study Design
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Study Design
We provide a telephone (IVRS) and web-based randomisation infrastructure for enrolling/randomising patients into randomised clinical trials.
Study-specific provision, including telephone charges, voice recordings and production, setup and administration of individual randomisation schedules will, however, be met by the individual study budgets.
Advice on the design and conduct of clinical trials
Protocol review and statistical methods sections
Sample size calculations and statistical analysis plans
CRF design: e-trial facility or in printable format
Preparation of randomisation schedules