Electronic Investigator Site File (eISF)
Clinevo electronic Investigator Site File (eISF) is a cloud based, easy-to-use and highly secured electronic document management platform for investigator sites involved in the clinical trial for full control over their investigator site files (ISF).
Clinevo electronic Investigator Site File (eISF) meets regulatory guidelines including:
Digital content archiving
Security and access control
Change controls
Audit trails, and System validation.

Comprehensive Pharmacovigilance Solution
Clinevo Pharmacovigilance Software is a powerful, AI-driven drug safety database designed to streamline case processing, ensure compliance, and provide advanced analytics for pharmaceutical companies, CROs, and regulatory teams.
Configurable ISF Structure
File Planning & Milestones Setup
Live Tracking of Missing Documents
Document Lifecycle and Version Control
Efficiency & Cost Optimization
Clinevo Safety is built on a simplified technology stack, ensuring cost-effectiveness, easy maintenance, and faster user adoption.
Advanced Analytics
Clinevo electronic Investigator Site File (eISF) System is the best eISF that provides advanced analytics to track Completeness, Quality, Timeliness and TMF compliance of a study.
Bulk / Quick upload
Clinevo electronic Investigator Site File (eISF) System allows users to upload hundreds of documents in one go using a simple drag and drop & provides dynamic indexing options for documents
Integration with eTMF
Clinevo electronic Investigator Site File (eISF) software can be integrated with the eTMF systems to automatically file selected documents into eTMF
Sharing and Collaboration
Clinevo electronic Investigator Site File (eISF) software allows a user to invite external parties to upload and work collaboratively on documents in a controlled manner
Smart Insights & Accessibility
Clinevo Pharmacovigilance Software offers intelligent analytics and real-time compliance alerts while ensuring seamless access from anywhere.