Core Modules

Quality Management, unified in one validated system

Accura brings core quality processes into a single controlled platform designed for regulated life sciences and laboratory environments. Each module is built to support auditability, traceability, and regulatory alignment while reducing manual administrative effort.

Document Control

Controlled documents. Always current. Always traceable.

Manage SOPs, work instructions, forms, and controlled records in a structured, validated document system.

Key capabilities:

Version-controlled document lifecycle
Multi-stage review and approval workflows
Electronic signatures compliant with regulatory expectations
Full audit trail of every change and revision
Controlled access based on roles and responsibilities

Ensure your organisation always works from the correct, approved version of every document.

Training & Competency

Ensure personnel are qualified and current

Maintain training compliance and competency tracking across roles, departments, and sites.

Key capabilities:

Automated training assignment based on role or SOP updates
Competency tracking and qualification records
Training completion evidence with full traceability
Real-time compliance visibility dashboards

Ensure staff readiness is maintained continuously, not just during audits.

CAPA Management

Structured investigations from issue to resolution

Manage deviations, non-conformances, and quality issues through a controlled CAPA workflow.

Key capabilities:

Structured deviation logging and classification
Root cause analysis tools (5-Why, Fishbone support)
Corrective and preventive action tracking
Effectiveness checks and closure validation
Full linkage to related documents, risks, and audits

Support consistent, defensible investigation processes.

Change Control

Evaluate and approve change before impact occurs

Control changes to processes, systems, materials, and documentation through structured governance.

Key capabilities:

Pre-change risk and impact assessment
Multi-level approval workflows
Validation and verification steps linked to change records
End-to-end traceability from request to release

Ensure regulated changes are properly assessed before implementation.

Risk Management

Identify, assess, and control quality risk

Maintain structured risk models connected to real operational data.

Key capabilities:

Configurable risk scoring frameworks
Hazard identification and classification
Residual risk tracking over time
Direct linkage to CAPAs, audits, and change controls

Maintain visibility of risk across your quality system.

Audit Management

Be continuously audit ready

Plan, execute, and manage internal and external audits with full traceability.

Key capabilities:

Audit scheduling and planning
Structured audit execution workflows
Finding capture and classification
Direct escalation into CAPA workflows
Audit history and readiness tracking

Reduce audit preparation effort and improve inspection confidence.

Supplier Quality Management

Extend quality control beyond your organisation

Manage supplier qualification, monitoring, and performance within a controlled framework.

Key capabilities:

Supplier onboarding and qualification workflows
Ongoing performance monitoring
Documented compliance and certification tracking
Supplier risk classification and review cycles

Ensure external partners meet your quality expectations.

One platform. All core quality processes.

Accura provides a unified system for managing quality operations in regulated life sciences environments—designed to reduce fragmentation, improve traceability, and support inspection readiness.

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