PHARMASEAL, a new provider of clinical trial management and governance solutions, announced that a U.S. health outcomes and technology company has selected Engility Clinical Trial Management system for the management and oversight of its clinical trial programs.
In the field of health outcomes and technology, companies are looking to leverage big clinical data and artificial intelligence (AI) to better understand, compare, and predict patient outcomes. The task of combining real-world evidence (RWE), clinical registries and AI technologies can be challenging. Engility was chosen to provide a validated system for managing clinical trial information, reduce data duplication and improve trial collaboration.
Engility CTMS is a modern cloud-based enterprise trial management system used by medical device, biopharmaceutical, and CRO’s to aim to improve how they manage and control clinical trials. With support for multiple sourcing models, flexible trial designs including centralized/virtual/remote trials, Engility CTMS is ideally placed to support good clinical practice (GCP E6) requirements and spearhead clinical operational process improvements.
Daljit Cheema, Founder and CEO of PHARMASEAL commented, “We are delighted that our integrated enterprise platform, Engility, has been selected and licensed to help drive new insights for this company. Our innovative platform utilizes advanced engineering offering enterprise management with rapid deployment, an intuitive user interface and interoperability with other eClinical applications to optimize governance and oversight. At PHARMASEAL, we have the vision to create smarter technologies for the improvement of human health and we are excited to see what possibilities emerge from this collaboration for transforming the future of healthcare.”
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.
Arcus’ Quemliclustat Earns Orphan Drug Designation as Phase III Pancreatic Cancer Trial Advances
July 11th 2025The FDA has granted orphan status to Arcus Biosciences’ CD73 inhibitor quemliclustat for metastatic pancreatic cancer, as the global PRISM-1 Phase III trial nears full enrollment following promising survival data from ARC-8.
QWINT-1 Trial: Once-Weekly Efsitora Matches Daily Glargine in Type 2 Diabetes Management
July 10th 2025Results from the Phase III QWINT-1 trial show that Eli Lilly’s once-weekly insulin efsitora is noninferior to once-daily glargine in reducing HbA1c among insulin-naïve adults with type 2 diabetes, offering a simplified fixed-dose regimen with fewer hypoglycemic events and less treatment burden.