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Streamlining Confidentiality Disclosure Agreements to Accelerate Clinical Research

Study startup delays represent a critical barrier impairing efficiency in clinical research timelines and our ability to ultimately serve patients. Tackling each contributing factor in this issue should be an effort we all engage in. The Site-Sponsor Consortium—a unique collaboration of sponsors, contract research organizations, institutional sites, and commercial sites—will unveil its inaugural whitepaper, which details actionable strategies to simplify and harmonize Confidentiality Disclosure Agreement processes across the industry. Consortium members will discuss the operational and ethical imperatives for reform, the value of master and bilateral agreements, and the collaborative journey that led to consensus-driven solutions. Attendees will gain insight into the practical steps needed to reduce study startup timelines and foster a culture of shared responsibility, transparency, and innovation in clinical research.

CEU: 1.00 ACRP

Speaker:

Earlier Event: April 26
Getting to Yes: How Sites Can Use Their Preferred Technology in Trials
Later Event: April 26
Building Trust in Clinical Research Through Literacy-First Community Engagement