As regulatory authorities place greater importance on trial oversight for clinical events, data monitoring and more, sponsors are turning towards external oversight committees to help strengthen trial strategy and framework to better protect patient safety and scientific quality within the trial process. IQVIA Clinical Events Validation & Adjudication (CEVA) will successfully design and deliver an effective and independent oversight group management and/or endpoint adjudication strategy while simultaneously managing the projected budgets.
IQVIA Clinical Event Validation and Adjudication (CEVA) offers sponsors an umbrella of scalable, cost-efficient, end-to-end committee management and adjudication support solutions through a global team of experts who are highly experienced and ready to guide your team through the committee planning, establishment, and implementation processes.
From standalone to full-service models, IQVIA CEVA's flexible solutions allow you to build a tailored strategy that fits your trial and/or program's needs.
