Every team has different jobs-to-be-done. Pick the one that sounds like yours — we’ll show you the exact configuration, KPIs and rollout plan.
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From mid-market pharma to CMOs, biotech startups and CROs — KOŚA delivers the same modern compliance backbone, configured to how your organisation actually works.
The complete module library
Every team has different jobs-to-be-done. Pick the one that sounds like yours — we’ll show you the exact configuration, KPIs and rollout plan.
Each solution comes with: pre-built templates, role-based dashboards, regulator mapping (FDA, EMA, CDSCO, WHO-GMP), and a 90-day rollout playbook.
Primary
For mid-market pharma stuck between expensive legacy contracts and risky Excel + SharePoint workflows.
Secondary
Operate multiple client programmes from a single, tenant-isolated platform.
Tertiary
For Series B/C biotech that needs enterprise-grade systems before the first FDA inspection.
Quaternary
Centralise training, documents and OJT attestations across multi-site studies.
Why teams pick KOŚA
Built for the regulator’s perspective, priced for emerging-market budgets, architected for distributed manufacturing.
Average rollout to first audit-ready state
Reduction in compliance management cost
Modules across the GxP lifecycle
21 CFR Part 11 e-signature coverage
We’ve configured KOŚA for hospital pharmacies, API manufacturers, medical device firms and more. Tell us your context — we’ll map it to the right modules.