Connected Records
Seamlessly link deviations to CAPAs, and CAPAs to document changes.
One connected quality system
From disconnected quality work to one connected operating system
Quality processes are easier to control when information, workflows, and records are connected across your quality system.
Shared Data
Eliminate redundant data entry across different quality processes.
Complete History
Maintain a comprehensive, traceable audit trail across the entire platform.
Centralised Visibility
Connect quality processes and records in one unified quality environment.
Modular by design
Start with core modules.
Add optional capabilities when needed
Core Quality Modules
Document Control
Manage the entire document lifecycle from creation to obsolescence.
Training & Competency
Automate training assignments based on document changes and role updates.
Deviations & CAPA
Investigate issues, determine root causes, and implement corrective actions.
Change Control
Evaluate, approve, and implement changes in a controlled, traceable manner.
Extended Capabilities
Risk Management
Identify, assess, and mitigate risks across operations.
Audit Management
Plan, execute, and manage internal and external audits with complete traceability.
Supplier Quality
Maintain oversight of supplier quality activities and documentation.
Additional Workflows
Extend the system as quality processes and operational needs evolve.
Document
Create Document
Review & Approval
Controlled Document
Training
Quality Event
Deviation
Risk Management
CAPA
Process Change
Change Request
Risk Management
Change Control
Document & Training
Effectiveness
Quality Audit
Audit
Findings
CAPA
Configured around how your organisation works
Adapt the system to your standard operating procedures, not the other way around. Define precise approval paths, granular permissions, and automated escalations without writing code.
Approval workflows
User roles & permissions
Review cycles
Notifications & escalations
Validation-ready foundation
Validation-ready foundation
for easier setup and faster adoption
Accura is built to reduce the effort required to implement and maintain a compliant quality system. With a validation-ready platform foundation and structured setup approach, teams can move from implementation to adoption with greater confidence.
Validation-ready platform foundationReduced validation effortStructured setup processControlled platform updates
Support for setup, documentation,
training and onboarding
Implementation Support
Expert guidance to configure the platform to your specific operational needs.
Documentation Support
Assistance with migrating and structuring your existing quality documents.
Training & Adoption
Comprehensive training programs to ensure smooth user adoption.
Validation & Consulting
Ongoing support to help manage validation activities as the platform evolves.
Built for regulated life sciences environments
Biotechnology &
Biopharma
Medical Devices
Pharmaceuticals
