Full cycle product for Research and Development teams in Pharmaceutical Industry. The product includes Electronic Trial Master File, Trial Management, Logistics and Inventory, Electronic Document Management with eSignature support. That is suitable for regulated areas as it is fully compliant with 21CFR Part 11 requirements.
Electronic Signature
Electronic File Management
Milestone tracking
Milestone, Tasks
Quality Control
Scheduling
Analytics and Reporting
Issue/Task Management Tools
Logistic Analytics
Shipment controlling
Calibration
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