02.17.25 -- The Scoop On SCOPE

Determining the feasibility of a site for clinical research is a critical component of the entire trial process. Discover how automation and standardization can improve the site-sponsor journey.

This overview highlights real research programs at various stages of the recruitment process, demonstrating the impact of Advarra’s Longboat Platform across multiple therapeutic areas.

Integrate data from all industry sources to confidently plan budgets for studies worldwide, across all phases and therapeutic areas.

Patient advocacy organizations (PAOs) play a pivotal role in rare disease research by bridging the gap between patient communities and biotech companies.

Patient-focused drug development (PFDD) is gaining traction as clinical trials increasingly prioritize patient perspectives alongside traditional endpoints.

Accelerate enrollment, improve timelines, and increase patient retention for your ophthalmic or non-ophthalmic trials.

Historically, the patient perspective was captured during site visits, paper diaries, and questionnaires. Review today's platforms for collecting electronic clinical outcome assessments.

Lynn Bartholow is transforming clinical research for Native American populations. Explore her journey into clinical research and efforts to build trust and foster participation and community engagement.

In order to capture the proper data points within an applicable study setting among a representative patient population, learn why appropriate patient recruitment strategies and execution are crucial. 

The FDA has issued multiple guidelines in recent years to enhance diversity in clinical trials. These efforts aim to ensure medical products are effective and safe for all populations.

Explore the innovative approach taken during this clinical trial partnership to address the underrepresentation of minority communities in clinical trials through digital storytelling.