01.13.25 -- How To Work With A Research-Naïve Clinical Trial Site

As the landscape evolves, sponsors must adopt innovative, patient-centered approaches and technologies to effectively conduct LTFU studies, minimizing the burden on patients and research sites.

Learn how a partnership with a pharmaceutical company to redesign patient support materials resulted in increased patient engagement and copay program utilization.

In this interview, Eric Klaver, IQVIA's DCT regulatory director, discusses how IQVIA supports investigators in decentralized clinical trials (DCT) compliance and operations.

See how this customized educational approach significantly enhanced recruitment and retention efforts, helping to ensure a more inclusive trial for Nonobstructive Hypertrophic Cardiomyopathy (nHCM).

Review several pertinent barriers that have impeded diversity in clinical studies and the strategies used to overcome them.

Explore effective strategies to enhance diversity and inclusion in clinical trials by supporting underrepresented patient groups, ensuring equitable health outcomes and broader representation.

Diagnostic studies can be designed in a multitude of ways. However, when it comes to reaching the desired patient pools, there are benefits to incorporating models with decentralized elements.

Choose the right software and digital advertising to target qualified patients for your clinical study and work alongside a team of local enrollment specialists assisting your recruitment efforts.

Creating a site-centric partnership between a pharmaceutical/biopharmaceutical sponsor and a clinical trial site can ease personnel and patient burdens, driving high-quality data collection and documentation.

Through an examination of evolving trial strategies and implementation, we aim to lay the groundwork for a collaborative, mutually beneficial atmosphere, ultimately leading to a sustainable competitive edge.

Uncover how this shared investigator platform optimizes resource allocation and ensures a more agile and responsive clinical research environment.