Product Overview
Centralized Document Management: eRegulatory systems centralize the management of regulatory documents, making it easier to organize, track, and retrieve essential files across multiple studies.
Improved Compliance: An eRegulatory solution helps ensure that all regulatory documents are kept up to date and meet the latest compliance standards, reducing the risk of non-compliance during audits or inspections.
Automated Workflows: With built-in workflows, an eRegulatory system can automate tasks such as document approvals, notifications, and audit trails, saving time and reducing administrative burdens.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
More Information
- Remote Access and Collaboration: eRegulatory solutions provide secure, remote access to regulatory documents, allowing study teams, sponsors, and auditors to collaborate and review documentation in real-time from any location.
- Reduced Risk of Errors: By automating version control and tracking document updates, eRegulatory systems reduce the risk of errors or outdated information being used during the trial.
- Audit-Ready at All Times: An eRegulatory system ensures that all documentation is audit-ready, with complete traceability and a detailed audit trail for every action taken within the system.
About the company
eClinPro, LLC is an American company with a SaaS workflow for the clinical research industry providing powerful tools as CTMS/ eSource/ eDocs/ Text that facilitate the clinical trials conductions improving compliance and efficiency.
