GlaxoSmithKline Standardizes on BioClinica Trident IWR Solution
BioClinica®, Inc., (NASDAQ: BIOC) announced that GlaxoSmithKline LLC (“GSK”) has signed a multi-year enterprise technology agreement to deploy BioClinica’s Trident IWR (Interactive Web Response) system across its Phase I-IV clinical trials.
“GSK had a requirement for a new solution to enable internal staff to configure and manage highly complex IWR clinical studies, and we are pleased GSK chose Trident,” said Mark Weinstein, CEO of BioClinica. “We look forward to supporting GSK so that they can successfully deploy and utilize our software in their upcoming studies.”
Trident IWR’s design provides clinical operations personnel with a way to directly set up, monitor, and maintain randomization and supplies for their clinical trials, in less time than previously required. Trident IWR delivers rapid study setup without the need for programming, while delivering IVR (Interactive Voice Response) system phone support through the same configuration process.
Unifying Industry to Better Understand GCP Guidance
May 7th 2025In this episode of the Applied Clinical Trials Podcast, David Nickerson, head of clinical quality management at EMD Serono; and Arlene Lee, director of product management, data quality & risk management solutions at Medidata, discuss the newest ICH E6(R3) GCP guidelines as well as how TransCelerate and ACRO have partnered to help stakeholders better acclimate to these guidelines.
FDA Grants Priority Review to Merck’s sBLA for Winrevair After Early Success in ZENITH PAH Trial
July 2nd 2025Merck’s bid to update Winrevair’s label advances with FDA priority review, backed by Phase III ZENITH data showing a 76% reduction in major morbidity and mortality events in patients with pulmonary arterial hypertension.
