AG Mednet Blog

Blog / January 8, 2019

At the end of November, Michael Causey, writing for the Association of Clinical Research Professionals,  quoted FDA Commissioner Scott Gottlieb saying “We don’t use technology well in clinical trials to collect information and to use it to do quality checks on the data that’s collected.”...

Blog / January 11, 2018

AG Mednet’s Brian Kelly joins experts from Oracle to address data quality and compliance in medical device trials during this upcoming webcast. The webcast – Adaptive Medical Device Trials for Fast, Seamless and Accurate Research – takes place Thursday, January 25, 2018, noon EST. Medical device studies...

Blog / January 10, 2017

In 2015, the Food and Drug Administration released the Clinical Trial Imaging Endpoint Process Standards draft guidance for the clinical trial industry. According to the FDA, the purpose of the guidance is to assist sponsors in optimizing the quality of imaging data obtained in clinical trials intended...

Blog / January 6, 2017

There are a number of challenges when designing and building solutions for the collection and delivery of image submissions for clinical trials. One of them is compliance with global regulations governing the process. While regulations set forth by agencies such as the FDA, HIPAA, and...