MedPoint Digital
eSafe provides a user-friendly interface with intuitive step-by-step functions. It’s so simple that no training is required for Investigators and site staff. eSafe is designed for efficient, rapid start-up and deployment. MedPoint provides comprehensive support so sites can validate and configure eSafe to their needs. To support the goal of paperless documents across the clinical trial landscape, Study eSafe is now available to study sites for all trials and all site users at no charge. Designed specifically for the clinical researcher at Research Study Sites and Research Institutions, Study eSafe is a validated, 21 CFR Part 11 compliant eReg/eSource system that provides a paperless solution to several challenges facing clinical study sites. Process, organize and store all of your regulatory binder documents more efficiently. Run audits more smoothly and reduce the redundancy.
Core Features
Document Control Features
  • Archiving & Retention
  • Collaboration Tools
  • Contract Management
  • Document Assembly
  • Document Capture
  • Electronic Signature
  • File Recovery
  • File Type Conversion
  • Security
  • Version Control
Pricing Type
Contact Vendor
Free Version
Payment Frequency
Quote Based
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Licensing & Deployment
  • Cloud Hosted
  • Web-based
  • Phone
Knowledge Base
  • Help Guides
  • Video Guides
  • Blogs
  • Webinars