Simplify Document Control to manage documents efficiently, stay compliant, and keep your team inspection-ready; without manual chaos.
Simplify Document Control to manage documents efficiently, stay compliant, and keep your team inspection-ready; without manual chaos.
In the life sciences industry, document control is essential for managing SOPs, work instructions, quality manuals, validation protocols, and other regulated content. It’s the backbone of your QMS – and a key part of staying compliant with FDA, EMA, ISO, and GxP standards.
Quality Forward’s eQMS helps you manage every stage of the document lifecycle – from creation to approval to archiving – without chasing email threads or worrying about version errors.
Store and manage controlled documents in a validated, single source of truth.
Ensure timely collaboration with fully traceable, version-controlled routing.
Stay audit-ready with support for FDA 21 CFR Part 11, ISO 13485, and EU Annex 11.
Store all SOPs, batch records, work instructions, and policies in one compliant system
Ensure teams always use the right version, with complete change history
Support multi-step approvals and cross-functional reviews with ease
Automatically assign training when documents are updated or released
Quickly generate document reports and demonstrate compliance during audits
Compliant with GxP, FDA 21 CFR Part 11, ISO 9001/13485, and more
Easily customize forms, workflows, and escalation paths – no IT needed
Purpose-built for startups, scale-ups, and enterprise life sciences companies
Built by experts who know FDA, EMA, GxP, and ISO expectations inside and out
Automatically detect high-risk areas and recurring incident patterns
Enterprise-grade infrastructure for speed, security, and stability
Meet global standards with validation-ready workflows and secure audit trails
Create from templates or upload existing SOPs, specs, or validation docs
Send to the right SMEs, QA reviewers, or management with built-in routing
Capture 21 CFR Part 11–compliant signatures and control access by role or site
Link documents to CAPAs, audits, change controls, and training
Easily retrieve any document and show full approval history on demand
