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In regulated industries, effective document control and a robust quality management system can help bring products to market faster, reduce the financial risk stemming from lost or incorrect information, and maintain compliance requirements. Document Locator® offers quality managers and document control professionals an efficient way to manage information according to regulatory standards in programs like ISO, FDA, HIPPA, Sarbanes-Oxley (SOX), and more.
Quality documentation like CAPAs, SOPs, non-conformance reports, employee training, work instructions, and other managed file programs are managed within a document control repository that provides for version tracking, approvals, notifications, policy administration, and more. Automated, defined workflows ensure the reliability and repeatability of key processes, eliminating the errors, delays, and duplications common in manual, paper-based processes.
Auditing is made more efficient with the ability to quickly retrieve all files and verify processes. Records can be quickly searched based on content and metadata, and files are easily organized and accessible for review. Auditors may only need to validate an automated process once; whereas that same operation may need to be audited as many as 25 times or more when the process is manual.
Define and automate repeatable process steps using document workflow with notifications and approvals.
Capture a history of all changes with document version control, and control who has access to version history.
Record approvals using digital signatures.
Manage and control access with flexible security options.
Audit logging captures a history of document actions.
Scan and convert paper to digital format with document scanning.