11.11.24 -- Overcoming Trial Barriers By Looking Through The Lens Of Product Adoption

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.

A recent FDA draft guidance aims to address health disparities and enhance data quality through action plans for greater inclusivity in clinical trials.

Learn about advancements in diffuse large B-cell lymphoma research and personalized care strategies.

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. 

TA Scan, a web-based clinical intelligence tool, addresses challenges associated with the intricacies of trial planning by evaluating and ranking trial and site data to bolster the clinical study workflow.

The financial management aspects of clinical research sites are crucial to maintaining profitability. In this text, we outline three pivotal areas your site will need to address.

IQVIA Technologies leaders answer questions from sponsors, sites, CROs, and tech vendors about their aggregation platform that provides single sign-on across sponsors, studies, and systems.

See how this shared investigator platform helps reduce redundant tasks associated with site selection and qualification and is enabling teams to work with sponsors in a central workspace.