Flexible, adaptive designs allow for accelerated development through the ability to rapidly declare one or more treatments superior, drop treatments for futility, or dynamically add new treatments to be tested.
#Medical writing services trial#
Today, the distinction between trial phases has blurred, with more flexibility in trial design - often combining multiple studies in a single, overlapping protocol. Our team of medical, biostatistical, and operational experts help you balance these sometimes-competing priorities. A balanced study designĪ well-designed protocol accounts for patient safety, data integrity, and operational feasibility. We bring clinical expertise to portfolio- and study-level planning - harnessing the power of data-driven insights, historical knowledge, database intelligence, and thorough scenario planning. This upfront risk evaluation informs the entire study plan. Evaluation begins with risks to critical data and processes, as well as country selection, site-specific variables, and data integrity. Throughout each of these stages, our team continually assesses risk to control it and adapt as we move forward. To best serve patients and clinical trial sponsors, we take a risk-focused approach to clinical trial design, planning, and execution. Produce the right data with a risk-based approach to clinical trials
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