Product Overview
eRegulatory systems centralize the management of regulatory documents. This makes it easier to organize, track, and retrieve essential files across multiple studies.
An eRegulatory solution helps ensure that all regulatory documents are kept up to date and meet the latest compliance standards. This reduces the risk of non-compliance during audits or inspections.
With built-in workflows, an eRegulatory system can automate tasks such as document approvals, notifications, and audit trails. This saves time and reduces 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Errors: By automating version control and tracking document updates, eRegulatory systems reduce the risk of errors or outdated information being used during the trial.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.
