World-class technology to help sponsors and CROs manage clinical events, from trigger to final adjudication in drug, biologic and medical device trials.
The automated workflow solution focused on the security and automation of data safety monitoring board (DSMB) activities throughout a clinical trial, enabling an accelerated and secure trial process.
The global, market-leading functionality necessary to collect clinical trial image data, ensure compliance, and apply automated QA processes to data.
Streamline and automate central eligibility review workflows to ensure a clinical trial has an accurate group of eligible patients enrolled within an appropriate timeframe.
Meet Source Data Review and Verification needs by at the site through data captured consistently, reliably and within a protocol-compliant manner.
About Us
AG Mednet’s technology solves critical problems for the pharmaceutical, biotechnology and medical device markets. As the leading partner for endpoint / adverse event adjudication and imaging data collection and QC, we work with the world’s top pharmaceutical companies and CROs.
About Us
AG Mednet’s technology solves critical problems for the pharmaceutical, biotechnology and medical device markets. As the leading partner for endpoint/adverse event adjudication and imaging data collection and QC, we work with the world’s top pharmaceutical companies and CROs.
Support
The AG Mednet Global Help Desk is available 24x7x365 to support users around the globe. Our call center fields the call, initiates the troubleshooting, and assigns an AG Mednet technical resource.
Available 24/7
Fast Support
Support
The AG Mednet Global Help Desk is available 24x7x365 to support users around the globe. Our call center fields the call, initiates the troubleshooting, and assigns an AG Mednet technical resource.
Available 24/7
Fast Support
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