12.09.24 -- PI Talks Recruitment And Trial Design For Multiple Myeloma Studies

As protocols and studies become more complex, using technology to offer sites in-depth expertise and guidance is more important than ever to launch studies on time.

Explore India's adoption of global best practices, 24/7 work cycles, and audit readiness to ensure high standards of Good Clinical Practice, attract more trials, and provide robust data to stakeholders.

How do payment systems affect site-sponsor relationships? George Kourtsounis of Bristol Myers Squibb and Casey Orvin of CenExel Clinical Research lend their expertise to this question and more.

Clinical research sites play a crucial role in data collection, patient interactions, and protocol procedures. Utilize this methodology for uncovering site enablement capability maturity.

Dive into the global capabilities of this genomics laboratory, from early discovery and biomarker development to late-phase trials and companion diagnostics.

Becky Vivian shares her inspiring story, offering readers valuable insights into the unique challenges faced by caregivers of rare disease patients.

Discover how strategic partnerships with patient advocacy groups can optimize clinical trials by leveraging their insights, expertise, and dedicated support.

The clock is ticking on the requirement for pharmaceutical companies to include FDA-mandated diversity action plans for pivotal studies in clinical trials.

Learn how innovative strategies like free health exams, community engagement, and a comprehensive patient database helped this project achieve rapid enrollment with a high level of patient diversity.