ISO 17025 & 21 CFR Part 11 Compliant

Quality Management, Simplified

The modern regulatory compliance platform for laboratories and manufacturers. Document control, CAPA, training, and audits — all in one place.

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Everything you need for compliance

Purpose-built for regulated industries

Document Control

Version control, approvals, and e-signatures

CAPA Management

8D methodology with root cause analysis

Training Records

Competency tracking and certifications

Internal Audits

Schedule, execute, and track findings

ISO 17025
Laboratory Accreditation
21 CFR Part 11
FDA Compliance
UK & EU
GDPR Compliant

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