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Product Suite
A regulated-operations platform: multiple solutions ship today as one governed stack, with a deliberate roadmap across training, quality, laboratory informatics (LIMS), and batch/production records (BRM)—without fragmenting identity, audit, or deployment every time you add a module.
Available now
Each module shares the same identity, licensing, and audit philosophy—so you validate one platform story instead of stitching best-of-breed tools with fragile integrations.
Identity, org & license control for regulated IT
Central administration for organizations, sites, users, roles, and product licensing—the control plane that keeps segregation of duties and governance consistent across every Novaqis module. Ideal when you need one backbone for multi-site pharma or cosmetic operations instead of siloed tools.
GxP document management & electronic records
Electronic document management for pharmaceutical, biotech, and cosmetic quality teams: controlled lifecycle, workflows, electronic signatures, training-aware states, and audit trails—designed around themes relevant to 21 CFR Part 11 and EU Annex 11. A strong fit when you are comparing validated DMS or GMP document control solutions and want deployment inside your own infrastructure.
Operational insight for compliant environments
Reporting and event-oriented analytics suited to regulated operations—so quality and IT leaders can monitor activity without weakening data residency or access boundaries. Works alongside Admin and DMS when you need traceability across the stack.
Intelligent agent for documents, data & instant answers
Nova AI is Novaqis’s AI agent layer: high-accuracy OCR for scans and unstructured files, natural-language to SQL so you can describe a report in plain English and get on-demand analytics against real database data, ad-hoc analysis and summaries grounded in your environment, and a chatbot that answers operational questions in seconds—plus an extensible roadmap of automations. Designed to sit alongside Admin, DMS, and Reporting under your governance and access rules.
We are intentionally building a full regulated-operations story— LMS, QMS, LIMS, and batch / production records (BRM)—under one identity, audit, and deployment model. Detailed roadmap pages ship first where we have the most design-partner momentum (below); other modules are on the home timeline and in product conversations.
Training assignments, competency evidence, and curricula tied to the same identity and documents as DMS—on our roadmap.
CAPA, deviations, change control, and audits connected to controlled records—not a separate silo—planned as the suite grows.
Whether you are evaluating live modules now or planning LMS, QMS, LIMS, BRM, or other roadmap work—our team can walk you through the full platform vision.
