02.24.25 -- Lab Manual Gaps: Sabotaging Data One Sample At A Time

IQVIA's Director of the Applied Data Science Center Greg Lever discusses patient-centricity and the benefits of flexible trial models driven by smart analytics.

Discover how Citeline’s robust datasets, combined with real-world data, inform intelligent site and investigator selection for a rare, autoimmune disease. 

Learn about patient travel solutions that streamline logistics and travel for clinical trial participants and caregivers, ensuring a seamless experience.

FDORA has reshaped the clinical trial industry's focus on diversity, requiring diversity action plans and encouraging innovative strategies like DCTs and diversity-based site selection.

Accelerating overall trial timelines is critical to minimizing the financial risk of a clinical trial, and a hybrid trial model could work to speed up your recruitment and improve retention.

Amid challenges during the COVID-19 pandemic, discover how recruitment was completed in three countries for a Sweden-based pharmaceutical company's phase 2b study.

Direct outreach to potential participants and communication with their healthcare providers is key to boosting trial awareness and participation, thereby achieving recruitment targets.

eConsent is transforming clinical research sites by addressing key pain points and streamlining processes for overburdened staff.

Sites juggle dozens of applications, which increases their workload and limits their capacity. Sites need an industry-wide single sign-on experience that brings key systems and applications under one roof.

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