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.
Regulatory Compliance With eCOAs
April 26th 2024In the fourth and final part of this video interview with ACT editor Andy Studna, Melissa Mooney, director, eCOA sales engineering, IQVIA discusses how the regulatory stance on electronic clinical outcome assessments has changed over the years and what it could look like in the future.
Including Women of Childbearing Age in Clinical Research
March 26th 2024In recognition of International Women's Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and Marie Teil, Global Head of UCB’s Women of Childbearing Age Program. They speak about the specific challenges women with chronic illnesses face when accessing appropriate treatment and participating in clinical trials, UCB's Women of Childbearing Age Program and it’s most successful strategies, and much more.
Improving Engagement While Maintaining Data Integrity & Validity
March 19th 2024In recognition of Women's Health Month, we're featuring this recent talk between Associate Editor Miranda Schmalfuhs and uMotif's Chief Product Officer, Julia Lakeland, discuss new technologies improving patient engagement and reducing the emotional and logistical burdens of participation, ethical considerations that should be addressed when implementing those technologies, while ensuring patient privacy, and much more.
