AG Mednet to Address Global Endpoint Adjudication Challenges

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 Validation for IQVIA, will address the complicated nature of adjudication […]

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AG Mednet’s Judi Chosen to Manage 45,000 Adjudication Endpoints and Adverse Events in the Last 24 Months

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 sponsors and CROs to manage clinical events from trigger to […]

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AG Mednet Achieves EU-U.S. Privacy Shield and U.S.-Swiss Privacy Framework Compliance

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 the highest levels of data protection available to its customers […]

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Learn About AG Mednet’s Endpoint Adjudication Technology at Leading Clinical Trial Events This Fall

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 technology innovation, AG Mednet is reimagining how endpoint adjudication can […]

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AG Mednet Launches Endpoint Adjudication Technology to Ensure Data Quality

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 data quality. Judi helps sponsors and CROs manage […]

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AG Mednet Introduces Longitudinal Analysis within its Submission Quality & Compliance Module

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 Mednet Longitudinal Analysis, now included in the AG Mednet Submission […]

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AG Mednet and Imaging Endpoints Partner to Set Clinical Trial Benchmark for Image Data Quality and Compliance

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 software for oncology, neurology, musculoskeletal and cardiovascular clinical trials.

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AG Mednet Announces First Clinical Trial Quality Control Software for QIBA Imaging Protocol 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 first technology to automate the process of verifying QIBA protocol compliance, saving sponsors time and money and making it easier for investigator sites to submit quality data. QIBA is an RSNA-sponsored initiative to advance quantitative imaging and the use of imaging biomarkers in clinical trials by reducing variability.

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AG Mednet Joins Forces with Netherlands-based CRO Cardialysis for Efficient Cardiovascular Clinical Trials

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 or expose subjects to unnecessary risky procedures due to data […]

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AG Mednet Introduces Remote, Non-DICOM File Systems for Clinical Trials, Improves Data Quality

AG Mednet has announced the availability of new capabilities to enable sponsors, CROs and core laboratories to take delivery of electronic trial data into configurable file structures residing either locally or in any of their network shares. This functionality provides higher-quality data and less delays, making it the most efficient method to collect and transfer Holter data, spectral-domain OCT and newer modalities not yet conforming to the DICOM standard.

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