Audits & Certification Readiness
The starting point of every engagement: walk the rooms and read the records that belong to them, cross-reference both against the target standard, and hand back a prioritized log of exactly what has to change before the real audit — each finding with the clause it fails and the place it actually starts.
From first walk-through to certification support.
Pre-Audit
Walk the rooms, read the records that belong to them, cross-reference both against the standard.
NCF Log
Prioritized findings — Critical / Major / Minor.
CAPA
Corrective action per finding, with owner and deadline.
Remediation
Tracked to close.
Audit & Support
Formal audit report, re-check, certification support.
Billing is milestone-based, tied to programme stages — not flat invoicing.
Every finding is Critical, Major, or Minor — never ambiguous.
Critical
Would fail the formal audit outright, or creates a direct product-integrity or patient-safety risk. Addressed first, always.
Major
A significant gap that has to close before certification is realistic — the bulk of most remediation plans.
Minor
Documentation or process refinement that doesn't block certification, but is flagged so it doesn't resurface at the next surveillance audit.
Every major standard a regulated facility needs.
GACP, EU-GMP Annex 7, CUMCS G.A.P., and DTAM-GACP — plus any other regulated-facility standard (food, cosmetics, medical device) via a facility-agnostic, cross-standard readiness matrix. Not limited to cannabis or pharma.