Management of Clinical Site Documents and Associated Processes
How we help
Standardize your different clinical research sites by eliminating paper binders
Simplify your clinical trial process and keep your clinical study documentation audit-ready with Agatha’s eISF solution for clinical trials. Make all your essential study documents remotely accessible and identify missing documents much more easily than by reviewing physical binders at each trial site.
Connect monitors and sites through remote monitoring
Agatha Remote Monitoring enables monitors and inspectors to review source files, take notes, and efficiently carry out their monitoring tasks. The application also allows for the creation and assignment of tasks to site administrators, including notifications and tracking, all within a 21 CFR Part 11 and HIPAA-compliant application.
Agatha Remote eISF Benefits
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Elevate quality and cut down costs with Agatha’s remote ISF solutionPlanning to diminish time and expenses associated with the monitoring of your clinical trial sites? Our eISF solution presents a superior model, negating the need for on-site visits and reducing the administrative burden. -
Bring uniformity to your clinical research sites with Agatha’s eISFUtilize Agatha’s eISF solution to simplify your clinical trial process, maintaining audit-ready essential study documents. Achieve remote access to all critical trial documentation and promptly identify missing records, ensuring a compliant conduct of your trials. -
Facilitate effective sponsor systems interaction with remote monitoring via Agatha’s eISFAgatha’s eISF solution empowers monitors and inspectors to review source files, make notes, and complete their monitoring tasks, contributing to an efficient clinical trial process. The application also facilitates the creation and assignment of tasks for site administrators, enhancing the communication between technology systems.
Main Features
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