Documents and records
Manage controlled documents through revision, review and approval. Keep a record of document changes.
Explore Documents and records Interfacing EQMS | Capability directory
QMS modules for connected quality work
Explore eight QMS modules that support controlled documents, training, investigations and corrective actions. Start with the capabilities your quality team needs to evaluate.
Document controlInterfacing eQMS
Documents and training
Keep controlled content up to date and give teams a way to track the training that goes with it.
Training management
Organize training activities, monitor progress and keep training records available for review.
Explore Training managementAudits and corrective actions
Capture findings and quality events, then track the investigation and the actions that follow.
Audit management
Plan and conduct internal and external audits. Record findings and escalate them to corrective action where appropriate.
Explore Audit managementCAPA management
Document root causes, corrective and preventive actions, responsible roles and action status.
Explore CAPA managementQuality events
Raise nonconformities, document their causes and track related action items.
Explore Quality eventsRisk, incidents and supplier quality
Give teams a place to track risk indicators, respond to incidents and follow up on supplier issues.
Risk and controls
Assess risks, prioritize mitigation plans and monitor risk and control indicators.
Explore Risk and controlsIncident management
Record incidents, support investigation and track actions for follow-up.
Explore Incident managementSupplier quality and SCAR
Track supplier nonconformities and collaborate on supplier corrective action requests.
Explore Supplier quality and SCARAcross modules
From audit finding to corrective action
When an audit finding needs corrective action, the team can move into CAPA to document the investigation, assign actions and track their status. Review the handoff in the audit workflow example.
See the audit-to-CAPA exampleFrequently asked questions
Choosing QMS modules
Which QMS modules support document changes?
Documents and records management supports version control, review and approvals. Training management can track related training when a procedure change calls for it.
What is the difference between quality events and CAPA?
A quality event records an issue such as a nonconformity. CAPA manages the investigation and corrective or preventive actions when the issue requires follow-up.
What does SCAR stand for?
SCAR stands for supplier corrective action request. It gives a quality team and its supplier a way to track a supplier issue and the proposed response.
An Interfacing demo
See the modules that fit your process
Tell Interfacing where your team needs better visibility, from document reviews to corrective action follow-up.
More from Interfacing
Explore the full platform and related resources on the main Interfacing site.
