Updating monitoring strategies and combining them with the latest technology can streamline clinical trial processes to generate higher quality data and increase patient safety, says Brett Wilson.

Data safety monitoring is required for all clinical trials, but the level, elements and scope of such monitoring vary widely based upon the design, objectives, risks and endpoints of the study. The ...

The Clinical Trials Research Pillar in the Division of Biostatistics is at the forefront of innovative clinical trial design ...

She has led PRIDE, one of IQVIA’s largest employee resource groups, and is dedicated to increasing sustainable clinical trial monitoring models for the industry’s future.

Icon has begun the integration of Medidata Clinical Data Studio into its clinical studies. This development makes Icon the first CRO to completely integrate this technology into its workflows. The ...

After review by the Data and Safety Monitoring Board, the dosing of OCU200 in patients with diabetic macular edema (DME) will ...

MALVERN, PA — Ocugen, Inc. (NASDAQ: OCGN) announced progress in its Phase 1 clinical trial for OCU200, a novel biologic ...

This program was supported through an independent medical education grant from Dexcom Medical Affairs. Experts discuss the key benefits of continuous glucose monitoring (CGM) technology compared with ...

The Phase 2a clinical trial is designed to evaluate the safety ... to the signs and symptoms of their ESLD. A data safety monitoring board monitors each cohort of patients (N=4) to evaluate ...

The first patients have been enrolled in the HEROES trial, exploring de-escalation of anti-HER2 therapy in metastatic HER2+ ...