Every quality process, one connected eQMS
QFacts brings document control, training, events and complaints, CAPAs, change control and regulatory compliance together, so every record leads to the next step.
Six modules, one quality system
Every subscription includes all six modules. Start with the process your team needs most.
Document Management
Draft, review and approve SOPs and work instructions with version history, electronic signatures and periodic review reminders.
Explore moduleTraining
Assign training automatically when documents are published or roles change, and keep audit-ready training records.
Explore moduleEvents & Complaints
Record deviations and complaints, assess their impact and start an investigation when an event calls for one.
Explore moduleCAPAs
Give every corrective and preventive action an owner and a due date, and verify that it worked before closing.
Explore moduleChange Control
Assess the impact of each change, route approvals by change type and risk, and keep a complete change history.
Explore moduleRegulatory Compliance
Map requirements from 21 CFR Part 11, EU Annex 11 and ISO standards, follow up on gaps and prepare evidence for audits.
Explore module
One connected system
Quality work rarely stays within one process. A complaint can lead to an investigation and a CAPA plan. QFacts keeps these records linked, so you can follow each decision from the first report to closure.
- Events and complaints lead into investigations and CAPA plans, and every link is recorded.
- Publishing a document can assign training automatically, so people work from the current version.
- Role-based access and a full audit trail across modules make records easy to show during an audit.
Put QFacts to work for 7 days.
Sign up directly and explore how QFacts connects your documents, training and quality workflows. Start with a process your team knows.