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2x Faster Certification
The only platform manufacturing teams need for ISO 9001, FDA 21 CFR Part 11, GxP, and 27+ other standards complete with expert consulting and audit preparation built in.
Enterprise grade security you can trust
Get Your Custom Compliance Roadmap
Scattered systems, duplicate work, audit panic
Unified platform, streamlined processes, always ready
Scattered systems, duplicate work, audit panic
Unified platform, streamlined processes, always ready
Embed quality objectives, document control, risk-based thinking, and continual improvement across your QMS.
Manage health and safety risks with structured incident tracking, hazard identification, and preventive actions.
Align with global EMS expectations through operational controls, compliance registers, and environmental impact tracking.
Maintain traceability, CAPA workflows, and design controls to meet medical device QMS and regulatory requirements.
Support aerospace-grade quality with nonconformance management, supplier oversight, and product safety controls.
Ensure technical competence with auditable calibration records, equipment management, and validated test methods.
Monitor energy use, set consumption baselines, and implement improvement actions to drive energy performance.
Track working conditions, grievance mechanisms, and supplier compliance to uphold social accountability standards.
Manage documentation, cross-reference requirements across standards, track CAPAs, and prepare for audits without switching systems.
Access compliance experts who help you prepare for audits, build your documentation, and close non- conformities.
Get matched with partner auditors and internal audit specialists to make sure you're fully prepared.
2x Faster
Our pre-built templates and expert guidance compress typical 12-18 month certification timelines.
Zero Disruption
Implement compliance processes that work with your existing workflows, not against them.
Seamless Growth
Add ISO 14001, AS9100D, or any new standard using your existing documentation foundation.