GLASGOW and BOSTON – September 6, 2018 – Global Clinical Trial Partners (GCTP) has chosen AG Mednet’s Judi as its sole technology provider to deliver its enhanced, rigorous, single-vendor endpoint adjudication services to its clients. GCTP’s independent adjudication offering focuses on management of clinical event committees (CECs). The company provides endpoint adjudication for clinical trials as well as bespoke clinical trial consultancy, with a team of world-renowned clinical trial experts and academics in concert with pharmaceutical industry experts.
With Judi, GCTP will deliver a robust end-to-end, technologically advanced adjudication solution for clients by implementing their expertise in a concise, reproducible and efficient set of workflow methodologies that have been tried and tested in dozens of projects over more than 25 years.
GCTP works collaboratively with clients to determine an approach that best suits their unique needs and handles development of the endpoint process from start to finish. The company manages all aspects of the CEC process from small, single-center to large multinational, multi-center studies. Specific to adjudication, through Judi, GCTP provides:
According to Professor Mark Petrie of GCTP, “AG Mednet’s Judi software is the perfect fit for our bespoke adjudication solutions. The flexibility of their software allows us to easily implement workflow that not only enhances endpoint data quality, but also makes the end-user experience positively enjoyable.”
AG Mednet’s Judi helps advance clinical trials, serving as the first comprehensive electronic endpoint adjudication system to manage workflow and ensure data quality. Judi is an integrated, cloud-based SaaS tool providing 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.
“Global Clinical Trial Partners is unique in a number of important ways. Not only have they published pioneering peer-reviewed articles in the most important journals in the world, but they have brought their clinical expertise to a level where sponsors can benefit from their experience. Their customer-centric approach to endpoint adjudication represents a breath of fresh air in the industry. Using Judi as the technology backbone to power their processes is a perfect solution to what is already among the most comprehensive, efficient and accurate approaches to adjudication,” said Abraham Gutman, president and CEO, AG Mednet.
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.