Judi helps sponsors and CROs manage clinical events from trigger to final adjudicationAG Mednet continues its drive to advance clinical trials with the launch of Judi, the first comprehensive electronic endpoint adjudication system to manage workflow and ensure data quality. Judi helps sponsors and CROs manage clinical events from trigger to final adjudication in pharmaceutical, biologic and medical device clinical trials. This groundbreaking product capitalizes on AG Mednet’s experience delivering software in support of zero-delay clinical trials. AG Mednet is a specialized, electronic data collection and submission service dedicated to increasing data quality and reducing queries in clinical trials.
“We built Judi to improve the endpoint adjudication process,” said Abraham Gutman, AG Mednet president and CEO. “This critical process in advancing clinical trials has long suffered from lack of automation and data quality challenges. Using Judi allows for cleaner project management, reduced queries and more expediency during endpoint adjudication, all while improving quality.”
Judi, an integrated SaaS tool, provides a level of flexibility that enables the implementation of the most complex endpoint and adverse event processes, translating into more easily managed projects, fewer queries, higher accountability and increased quality throughout. Judi serves four distinct stakeholders across the endpoint adjudication spectrum:
From improved and automated workflows, to eCRF integration, electronic voting, dossier management and robust reporting, Judi eliminates the need for face-to-face meetings and streamlines the entire adjudication process. The introduction of Judi also adds these key features:
For more information about AG Mednet’s Judi and to learn how to work toward zero-delay clinical trials, please visit www.agmednet.com.
About AG Mednet
AG Mednet is the leading quality compliance partner for image data submission and collection, as well as endpoint and adverse event adjudication workflows. The company is a proponent of zero-delay clinical trials. The company has supported more than 850 global imaging trials. Dozens of adjudication protocols are being managed by sponsors and CROs using Judi. More than 45,000 registered users across thousands of investigator sites in more than 80 countries use AG Mednet to submit more than 10,000,000 images per month and adjudicate hundreds of events in projects sponsored by each of the world’s top 20 pharmaceutical, biotech and medical device companies.
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.