What we build
Novaqis Technologies is building a governed stack for regulated operations: live capabilities around enterprise administration, document control, operational reporting, and AI on governed data—with a roadmap across LMS, QMS, LIMS, BRM, and adjacent modules. The goal is buyer-led evaluation, deployment inside your perimeter, and validation-friendly design—not a patchwork of unrelated SaaS tools.
Who we serve
Our focus is organizations subject to GxP expectations—pharmaceutical and biotech companies, cosmetic GMP manufacturers, and quality-intensive operations that care about 21 CFR Part 11 and EU Annex 11 themes, ALCOA+ records, and audit-ready workflows.
How we work
Product decisions emphasize traceability, controlled documents, electronic signatures where appropriate, and clear separation of duties in partner-facing tools such as Novaqis Studio (licensing, quotes, support ticketing, and customer portals).
Contact & next steps
For demos, procurement, or partnership: contact@novaqis.com or use the contact section on the homepage. Licensed customers can sign in via Studio login and use the support overview for how ticketing and SLAs work.
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