AG Mednet Press Releases
DUBLIN–(BUSINESS WIRE)–ICON plc (NASDAQ: ICLR), a global provider of drug development and commercialisation solutions and services, today announced it has signed an agreement with AG Mednet to use Judi, a comprehensive electronic endpoint adjudication system to manage workflow and ensure data quality, for enhanced endpoint...
AG Mednet is presenting at the 4th Annual Endpoint Adjudication Conference taking place from May 1 to 2. The session titled “Overcome Global Endpoint Adjudication Challenges,” co-presented by Abraham Gutman, founder and president of AG Mednet, and Alisa Hummings, Global Head of the Clinical Event...
AG Mednet is making significant progress in providing needed technology for endpoint adjudication in clinical trials, now chosen to manage more than 45,000 adverse events. Judi, the first comprehensive electronic endpoint adjudication system to manage workflow and ensure data quality, is AG Mednet’s solution for...
Taking steps to further enhance medical data protection, AG Mednet is now EU-U.S. Privacy Shield-Certified and U.S.-Swiss Privacy Framework compliant via self-certification. AG Mednet technology is used in clinical trials in more than 80 countries including most European Union nations. The company is committed to...
BOSTON – October 27, 2017 – As part of its mission to move the clinical trial industry even closer to the goal of zero-delay clinical trials, AG Mednet will both attend and exhibit at several key industry events this fall. A leader in clinical trial...
Judi helps sponsors and CROs manage clinical events from trigger to final adjudication Boston, MA – May 2, 2017 – AG 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...
Boston, MA – June 8, 2015 – AG Mednet, creator of the first quality assurance software built specifically to detect errors at the investigator site prior to data submission, adds an industry-first – automated software that checks data across subject visits, at the source. AG...
AG Mednet and the board-certified, fellowship-trained radiologists at Imaging Endpoints believe strongly that every clinical trial data point counts, from pre-clinical through FDA submission. To support its guarantee of accuracy, compliance, real-time reads and sponsor confidence, Imaging Endpoints is utilizing AG Mednet’s Submission Quality and Compliance...
Clinical trial sponsors working to standardize the capture and submission of complex imaging data through new QIBA imaging charters now have an easy and effective way to ensure the protocols are being met. AG Mednet’s Submission, Quality and Compliance (SQC) software for QIBA is the...
Boston, MA and Rotterdam, The Netherlands – February 26, 2014 – Speed, efficiency and accuracy are vital to the success of clinical trials. With large amounts of data collected and significant room for data submission errors, there is even greater potential to disqualify participating patients...