For procurement & QA leaders
A regulated-operations platform built for how serious evaluations actually run
Novaqis is an independent suite—live modules for governance, documents, reporting, and AI on your data, plus a roadmap across lab, training, quality events, and production records. Our leadership comes from years of delivering and operating large-scale GxP quality and document platforms—the same category of systems enterprises buy from the incumbent suite vendors you already know. We started Novaqis to prioritize deployment flexibility, unified audit identity, and architecture without inherited constraints—then let your matrix and POC prove the difference.
What we believe: teams that run a disciplined side-by-side will see a generational gap in how the stack feels—speed to value, ownership of data, and honesty of integration—not because we say so, but because you test it the way you already test everyone else.
Why teams put Novaqis next to the usual enterprise shortlist
- Practitioner-shaped — Built by people who carried validation, releases, and production operations for regulated suites—not slideware.
- One platform story — Identity, licensing, documents, reporting, and AI share governed boundaries so you are not re-proving a new integration every quarter.
- GxP-minded — 21 CFR Part 11 and EU Annex 11 themes, ALCOA+ expectations, e-signatures—stated honestly as shared responsibility with your QA org.
- Deployment you control — Run where your regulators and security model expect—not where a vendor’s tenancy model forces you.
- Roadmap that matches the suite vision — Training, quality events, lab, and batch-record directions without abandoning the same audit vocabulary.
Use your existing matrix—we like a fair fight
Whether your incumbent is a widely adopted multi-tenant suite, a legacy DMS, or a stitched best-of-breed stack, apply the same criteria: lifecycle, obsolescence, training linkage, search, reporting boundaries, export and segregation-of-duties rules, validation packs, commercial model, and how AI touches production data. We publish module-level detail so your SMEs can map requirements without a generic deck—and we are comfortable with transparent, criteria-driven comparisons.
Common questions
- Is Novaqis an alternative in the same evaluations as major enterprise GxP suites?
- Often, yes. Buyers shortlisting regulated document management, GxP content systems, or multi-module quality platforms can evaluate Novaqis on the same functional, validation, and commercial criteria. We are a separate product; see our FAQ for how we refer to other vendors’ trademarks (identification only).
- Why does Novaqis sound confident versus legacy suite vendors?
- Our team has spent years shipping and operating large-scale regulated quality and document platforms—so we optimize for architecture, deployment choice, and lifecycle cost we wished we could prioritize earlier. That is our opinion and experience, not a universal benchmark; your POC and IQ/OQ/PQ decide fit.
- What should we score in an RFP or matrix?
- Use the same rigor you already use: 21 CFR Part 11 and EU Annex 11 themes, audit trails, e-signatures, release and obsolescence, training linkage, reporting boundaries, validation evidence, deployment model, and total cost of ownership. We welcome structured comparisons.
- How does Novaqis differ from a generic ECM?
- Novaqis targets pharma, biotech, and cosmetic GMP—controlled documents, accountability, inspector-ready evidence—not generic file sharing. Nova AI is scoped to your governed data (OCR, NL-to-SQL, Q&A), not a disconnected consumer-style chat layer.
- Where is the technical depth?
- Start with the products hub and DMS, then Admin, Reporting, and Nova AI. For a live walkthrough, contact us—we prefer demonstrating the stack over generic slides.
See the stack on your terms
Bring your requirements and risk questions—we will walk the live product and stay concrete.