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Agatha Remote eISF Benefits

Medical Device Company, Optos, Amps up ClinOps with Agatha Applications

Main Features

Craft separate, protected areas for each Site to handle its documents. Each site and study incorporates a complete set of placeholders for expected eISF documents. Apply configurable auto naming to maintain naming conventions adhering to trial standards and facilitate compliant document management.
RM General View
View all your workspaces for each clinical trial site in the dashboard and quickly see and access tasks assigned to you. Use the configurable views to inspect, verify, and identify gaps in the expected eTMF contract at any time.
Agatha Dashboard Workspace
Share binder contents (investigator site files, or eISF) in real time among monitors, sites, and sponsors. This enables remote document review and quality check in your clinical trial process, crucial for maintaining a steady flow of documents between sites. Utilize forms to communicate monitor notes and assign tasks to site personnel.
Pinpoint documents for the quality check process and track the quality review using custom views. Take advantage of workflows with electronic signatures to meet all compliance requirements. Establish automated workflows to transition final clinical study documents to the Master TMF. Our eISF solution offers a secure document exchange platform that aligns with documentation requirements and trial conduct standards, boosting your trial oversight capabilities.

Customer implementation examples

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