With the increased significance of patient scans as surrogate endpoints in clinical trials, the ability to collect imaging data that meets protocol requirements is more important than ever before.

Ensuring that image data is properly de-identified, case report forms are consistent with the images they complement, and scans meet protocol criteria, are all critical elements necessary to maintain the quality of timepoint submissions.

Enter AG Mednet.

AG Mednet offers the world’s largest 21 CFR Part 11, GCP and HIPAA compliant medical imaging network. Pharmaceutical, biotech and medical device companies, core labs and clinical research organizations (CROs) collecting imaging time points as part of their trial protocols, rely on AG Mednet’s automated system to enable the secure electronic transfer of scans from thousands of locations around the world, enhancing site compliance and reducing site queries, while providing the detailed reports necessary to meet the most stringent regulatory requirements.

AG Mednet is the only dedicated electronic image collection service that provides investigator sites all the workflow management tools and functions necessary to streamline their submissions while increasing compliance with all regulatory and protocol requirements. Additionally, with AG Mednet, sponsors and core laboratories see a measurable reduction in both logistical tasks and trial queries, leading to operating cost reductions and better outcomes.

AG Mednet is the image management service of choice in more than 200 global clinical trials. Over 8,500 registered users, across thousands of investigator sites in 58 countries, are using our service to participate in projects sponsored by every one of the Top 20 pharmaceutical, biotechnology and device companies in the world.

Contact us to learn more about how AG Mednet can help to optimize the efficiency of your imaging intensive clinical trial.