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...

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,...

To make trials more efficient and ensure compliance, syneed medidata GmbH, an independent CRO in Germany, has signed a Master Services Agreement with Boston’s AG Mednet....

Improved quality-control measures in clinical trials are gaining traction. AG Mednet driven by its mission of quality at the source for image-intensive trials helps sponsors and core labs comply with the FDA’s newly stated guidance. ...