Operational escalation
management for GMP teams
OgmaQ helps pharma and biotech quality and manufacturing teams capture, triage, assign, track and close every operational escalation — one structured, auditable workflow from first signal to a closed record.
Or email hello@ogmaq.com directly.
One workflow, from raised to resolved
Every escalation moves through the same auditable path. Everyone sees the same state, ownership and SLA health — no scattered spreadsheets, no informal follow-ups.
One source of truth, every seat at the table
Manufacturing raises and contains, QA assesses and approves, leadership sees the whole picture — the same record, the right view for each.
Manufacturing & Ops
Raise an issue in seconds, log containment, and hand over cleanly between shifts — nothing lost at the boundary.
Quality Assurance
Screen, triage and approve against a consistent rubric. Closure is held until every required gate is genuinely met.
Site Leadership
See risk and flow across every site and shift at a glance — where things stall, what's overdue, what's ready to close.
Isolation at the database, roles at the surface
Frontend permissions shape what each role sees; the isolation boundary is designed around database Row-Level Security. Multi-site, multi-tenant foundations with an append-only audit trail on every action.
Built for regulated operations
OgmaQ is an operational prototype, not a validated GMP/QMS system — it makes no 21 CFR Part 11 / EU Annex 11 compliance claim. Formal containment and release records stay in your validated QMS.
Bring every escalation into one place.
See how OgmaQ replaces scattered spreadsheets and informal follow-ups with one auditable workflow.
Or email hello@ogmaq.com directly.