08.12.26 -- eTechnologies Improving Trial Design And Execution

Sponsors depend on sites to recruit patients, execute protocols, and collect high-quality data. In this candid panel discussion, we explore what makes sites want to work with a sponsor.

Learn how clear workflows, proactive support, and accessible technology help translate services into real participant retention.

Global clinical trials increasingly rely on electronic consent, and inconsistent country signature rules can raise compliance risk. Learn a repeatable framework for inspection-ready eConsent.

Accelerate your trial startup and reduce site burden with a central eSource allowing sponsors to develop and publish central source templates to sites.

Leveraging primary care for chronic disease studies can accelerate patient identification, access to underrepresented populations, and improve retention rates.

Discover how functional service providers (FSPs) are reshaping clinical research by offering specialized expertise, flexible resources, and cost-effective solutions.

Expert perspectives on IRB oversight, health literacy, and research ethics offer practical guidance to strengthen consent, protect participants, and align compliance with real-world research.

Leida Bowen explains how patient councils and early community input can inform protocol design, reduce burden, and ensure trials reflect patient needs before study execution begins.