Controlled Documents, Closed-Loop Approval

Synesis QMS Document Management replaces shared drives, email approvals, and forgotten revisions with a single controlled library. Every SOP, work instruction, form, specification, policy, manual, and external document moves through a configurable Draft → In Review → Pending Approval → Effective lifecycle. Reviewers and approvers receive notifications in-app, by email, and inside Microsoft Teams — and decisions sync back automatically, so a status change in any channel updates the record.

Once a document becomes Effective, it lands in the Published Documents Library where the right people can find it instantly and the right people get a Read-and-Understand task. AI assists with description enhancement, classification, and review routing, while a complete audit trail records every change, signature, and timestamp. Native integration with SharePoint, Teams, Outlook, Azure, Power Automate, and Microsoft Copilot, on a modern Microsoft license-free platform. Deploy where you want — on-premise, on Microsoft Azure, on Amazon Web Services, or on the hosted solution of your choice.

Synesis QMS Document Library with status workflow and review/approval lifecycle
Document Library — manage controlled documents through the ISO 9001 review and approval workflow.

Document Control Capabilities

Controlled Document Library

Single Source of Truth

All controlled documents — SOPs, Work Instructions, Forms, Specifications, Policies, Manuals, Procedures, Record Templates, External Documents — managed in one library with type, owner, reviewer, approver, and retention period.

Review & Approval Workflow

ISO 9001 Compliant

Draft → In Review → Pending Approval → Effective. Configurable per document type. Reviewers and approvers get notified in-app, by email, and via Microsoft Teams. Rejection sends documents back with comments.

Version History & Revision Control

Complete Traceability

Every revision is preserved with its content, reviewer, approver, decision, and timestamps. Compare any two versions side-by-side. Effective documents move to the Published Library with the previous version marked obsolete.

Published Documents Library

Read-Only, Searchable

Effective documents only. Sorted by published date. Searchable by type, owner, department, tags. End users always see the current effective version with no risk of accessing draft or obsolete content.

Read-and-Understand

Acknowledgments & Evidence

Assign acknowledgment requirements per document. Track who has read and understood, who hasn't, and when. Each acknowledgment recorded with user, version, and timestamp. Audit-ready evidence on demand.

AI Description Enhancement

OpenAI-Powered

One-click AI assistant to expand, rewrite, reformat, or summarize document descriptions. Generate learning objectives, outlines, and standardized language. Preview before applying.

Retention & Confidentiality

Compliance Controls

Per-document retention period (years), confidentiality level (public, internal, confidential, restricted), and review interval. Automatic notifications when documents are due for periodic review.

Document Process Analytics

Lifecycle KPIs

Dashboard tracking total documents, documents in approval, average review time, average approval time, average total cycle, first-pass approval rate, overdue reviews, and reviews due in next 30 days.

ISO 9001 Document Control — Built In

ISO 9001 §7.5

Documented Information — creation, update, control of documents, and retention. Full lifecycle workflow with audit trail and electronic signatures.

FDA 21 CFR Part 11

Electronic records, electronic signatures, audit trail, and access controls. Validated workflow with user authentication and decision logging.

IATF 16949

Document and record control with revision history, distribution control, and read-and-understand for affected personnel.

AS9100 / ISO 13485

Aerospace and medical device document controls. Configurable confidentiality, retention, and approval routing per document type.

See Document Control in Action

Watch Synesis AI eQMS Document Management run a real ISO 9001 review and approval cycle. We'll demo it on your processes, with your roles.

Request a QMS Demo