Affordable, integrated EDC

agCapture is a proven EDC solution, used by leading pharmaceutical companies and clinical research institutions worldwide. As clinical trials become more complex, (number of simultaneous trials and locations), agCapture integrates advanced decision support to improve trial execution, investigator acceptance and trial outcomes. It supports trials in all phases, and scales from a single site to multiple sites and large international trials. agCapture can also support the needs of any growing company since it is delivered as a hosted / managed offering, reducing the need to invest in software, hardware and additional infrastructure support staff.

Seamless Integration with Safety Systems

agCapture provides seamless integration with the rest of the Aris Global suite of products including:

This integration allows organizations to achieve enterprise-wide support across all clinical operations and processes using a standardized platform. Companies can reduce their need for serious adverse event (SAE) reconciliation and increase efficiency while maintaining compliance.

As with all Aris Global products, agCapture is available as a hosted solution on the agOnDemand platform. For more than four years, agOnDemand has been providing best-in-class, cloud-based services to life science companies to help them meet their regulatory requirements without the pressure of maintaining sophisticated IT infrastructures.

agCapture integrates with Aris Global's leading pharmacovigilance system, ARISg, to eliminate the need for SAE reconciliation. Clinical trials can be managed seamlessly from start to finish by taking advantage of the detailed integration agCapture offers with any CTMS, including agClinical. Other key features include:

agCapture, which is based on a combination of Aris Global and InferMed software, enables organizations to take advantage of the benefits that a proven EDC system offers while considerably lowering costs. A proven solution, agCapture, has been used in hundreds of trials by leading pharmaceutical companies and clinical research hospitals, facilitating each user's daily clinical trial responsibilities.