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Complify QMSISO 9001 : 2015ISMS Integrated

Quality Management
That Actually
Gets Managed.

Complify QMS takes your organization from initial gap assessment to ISO 9001 certification — and keeps your quality program continuously audit-ready. Fully integrated with Complify ISMS, so security and quality share a single platform.

1M+
Certified orgs globally
HLS
Shared with ISO 27001
2015
Current standard
QMS Dashboard● Active
Clause Coverage96%
Quality Objectives88%
CAPA Closure Rate94%
4
Open CAPAs
2
Audits Due
98%
On-time Delivery
0
Critical NCRs
Platform Capabilities

Every QMS requirement.
One platform.

Complify QMS covers the full ISO 9001 lifecycle — from initial context analysis and quality policy through operational process management, nonconformity handling, and continual improvement.

🎯
Quality Objectives Management

Define, track, and report quality objectives at organizational, departmental, and process level. Link objectives to measurable KPIs with automated progress tracking and management review dashboards.

📋
Process Management

Document and maintain your process landscape with turtle diagrams, SIPOC models, and process interaction maps. Version control, approval workflows, and distribution tracking included.

🔍
Nonconformity & CAPA

Capture and classify nonconformities, customer complaints, and internal findings. Drive root cause analysis and corrective actions through to verified closure with a full audit trail.

😊
Customer Satisfaction

Manage customer feedback, track satisfaction trends, and link customer-identified issues to corrective actions. Demonstrate your commitment to customer focus with structured evidence.

⚖️
Risk-Based Thinking

Identify and assess risks and opportunities at context, process, and product level. Develop treatment plans, track effectiveness, and integrate risk management into your management review.

Internal Audit Programme

Schedule and manage your ISO 9001 internal audit programme. Assign auditors, generate checklists, record findings, track NCRs to closure, and produce management review inputs automatically.

Clause Coverage

Every clause. Automated
where it matters most.

Complify QMS provides workflow automation, document templates, and evidence collection for every operational clause of ISO 9001:2015.

§ 6.1
Actions to Address Risks

Risk-based thinking embedded in every quality process — identify, assess, and treat risks and opportunities systematically.

§ 7.1
Resources & Competence

Track resource allocation, staff competence, training records, and infrastructure requirements aligned to your quality objectives.

§ 8.1
Operational Planning

Plan and control processes needed to meet product and service requirements — with documented criteria and evidence of conformity.

§ 8.4
External Providers

Manage supplier qualification, monitoring, and performance evaluation. Maintain a supplier register with documented criteria and review cycles.

§ 9.1
Monitoring & Measurement

Define what to monitor, how to measure, and when to analyse. Complify automates data collection and generates performance reports for management review.

§ 10.2
Nonconformity & CAPA

Structured nonconformity management from capture through root cause analysis, corrective action, and verified effectiveness review.

Certification Journey

From gap to ISO 9001
certified — with a plan.

Complify QMS guides your team through every phase of ISO 9001 certification with structured workflows, pre-built templates, and a dedicated implementation specialist at each step.

1
Phase 1 · Weeks 1–2
Context, Scope & Quality Policy

Define your QMS scope, analyse internal and external context, identify interested parties and their requirements, and establish your quality policy with measurable objectives.

Scope DefinitionContext AnalysisQuality Policy
2
Phase 2 · Weeks 3–5
Process Mapping & Risk Assessment

Document your process landscape, identify process interactions, conduct risk-based thinking assessments, and define control criteria for all operational processes.

Process MappingRisk AssessmentProcess Interactions
3
Phase 3 · Weeks 6–11
Documentation & Implementation

Develop required documented information — procedures, work instructions, quality records. Implement processes, conduct training, and begin collecting conformity evidence.

DocumentationStaff TrainingEvidence Collection
4
Phase 4 · Weeks 12–13
Internal Audit & Management Review

Run your internal audit programme across all clauses. Manage findings and corrective actions. Complete a formal management review with all required inputs and outputs documented.

Internal AuditCorrective ActionsManagement Review
5
Phase 5 · Certification
External Audit & Certification

Provide your certification body structured access via the Complify auditor portal. Achieve ISO 9001 certification and maintain continuous readiness for surveillance audits.

Auditor PortalCertificationSurveillance Ready
Get Started

See Complify QMS in action.

Our specialists will walk you through a tailored demo — showing how Complify QMS fits your organization's processes, certification goals, and existing management systems.