100% Free Complete GxP Software Suite for Emerging Pharma & Startups
Achieve urgent regulatory readiness for CDSCO Revised Schedule M, US FDA 21 CFR Part 11, EU GMP Annex 11, and WHO GMP. Qualifying emerging pharma, loan-licensees, and biotech ventures receive 12 months of free enterprise production licenses across ALL Novaqis Applications with zero per-seat user taxes and automated CSA validation packs.
Legacy Monopoly vs Catalyst Grant
Two Specialized Global Qualification Tracks
Whether you are an Indian formulation manufacturer facing the CDSCO Revised Schedule M inspection deadline or a venture-backed global biotech preparing clinical FDA submissions, Novaqis Catalyst has a dedicated pathway for your plant.
Engineered for Indian Small & Midsize Pharma Plants
Designed specifically for Indian formulation plants, API synthesis blocks, sterile injectables, loan-licensees, and export manufacturers racing to meet statutory state and central Schedule M inspection deadlines without enterprise software price gouging.
ALL 12 Enterprise Applications Available Under Catalyst
No stripped-down trial software. Qualifying ventures get production-grade access to any or all of our 12 integrated applications tailored to your facility roadmap.
21 CFR Part 11 document lifecycle, competency training, deviations & CAPA
In-browser collaborative authoring with real-time track changes, cryptographic signatures, and zero MS Word seat tax.
- Pantograph anti-photocopy print security
- Serialized copy distribution (Copy 1 of 5)
- Global Master SOP harmonization across facilities
- ALCOA+ immutable revision audit trails
Presence-verified workforce training with WASM dwell gates, AI question banks, and sterile cleanroom voice observation.
- Zero-hardware Cleanroom Voice OJT sign-off
- WASM attention timer (minimum 45s dwell)
- Automated SOP revision retraining sync
- 11 Indian & global localization languages
Closed-loop deviation, non-conformance, and market complaint investigation with automated Ishikawa and 5-Why root-cause trees.
- ICH Q9 risk matrix scoring
- Governed Change Control impact assessment
- Automated LMS retraining assignment gates
- Instant cryptographically signed 483 response packs
24/7 continuous autonomous surveillance scanning 30+ ALCOA++ compliance rules across documents, tests, and training.
- Rapid quiz & shared credential anomaly detection
- Dedicated Inspection Room mode with watermarks
- Forensic cross-modular timeline reconstruction
- One-click cryptographically sealed PDF evidence
Calculate Your Facility's Catalyst Grant Value
See the exact capital your emerging plant or biotech preserves in Year 1 by deploying Novaqis Catalyst instead of paying legacy vendor monopolies.
Equivalent to ~₹174.7 Lakh INR in capital preserved
*Note: Professional validation services (CSV/CSA), custom protocol qualification, and Annual Maintenance Contracts (AMC) involve specialized engineering effort and are evaluated per facility requirements.
Apply for Catalyst GrantFrom License Grant to Plant Go-Live in 48 Hours
Legacy implementations take 6 to 9 months of vendor billing. Novaqis Catalyst leverages autonomous configuration to launch in days.
Submit Facility Profile
Complete the 2-minute application below with your plant details, user allocation, and compliance inspection goals. Our team confirms eligibility within 1 business day.
Autonomous URS Introspection
Deploy on your plant network server or sovereign cloud. The Autonomous CSA Engine introspects your licensed modules and auto-shapes qualification test protocols to your intended use.
Audit-Ready Plant Launch
Begin authoring SOPs, running QC formula worksheets, and recording cleanroom logs. Automated IQ, OQ, PQ, RTM, and VSR binders stand ready for state, central, or FDA auditors.
Apply for Novaqis Catalyst License Grant
Provide your organization details and desired modules. Our compliance engineering team verifies eligibility and issues your cryptographic license envelope within 1 business day.
Frequently Asked Questions
Are ALL Novaqis Applications really included free of cost?
Yes! The Novaqis Catalyst Program covers ALL Novaqis Applications—including DMS, LMS, QMS, LIMS, CVM™ (Cleaning Validation), BRM (Electronic Batch Records), eLog™, Lab Digitize, AuditLens, ERP/HRMS, and the Autonomous Validation Engine. You can deploy the complete integrated suite or choose the specific applications required for your facility's current phase with zero software license fees for 12 months.
Why is Novaqis offering free licenses to smaller and newer pharma?
We believe quality and patient safety should never be compromised by multi-million-dollar legacy software monopolies. In India, the CDSCO Revised Schedule M mandate poses an urgent compliance deadline for MSME manufacturers who cannot afford legacy enterprise tools. Globally, early-stage biotechs risk FDA 483 audit observations by relying on spreadsheets. By equipping emerging leaders with world-class GxP infrastructure from Day 1, we build lasting partnerships that scale as your production and market footprint expand.
Do we need to enter credit card or payment information to apply?
No. Zero payment information, bank details, or credit cards are required. You submit your basic facility profile and receive a cryptographically signed ES256 license token directly after eligibility verification.
Is this a stripped-down trial or full production-grade software?
This is 100% full production software. Catalyst grants include unthrottled access to production capabilities: 21 CFR §11.50 cryptographic e-signatures, immutable ALCOA+ audit trails, ASTM E29 formula worksheets, 6-state cleanroom FSM logbooks, and continuous automated CSA validation.
What happens after the initial 12-month period?
If your organization still meets the program eligibility criteria (turnover under ₹10 Crore in India or under $5M funding / $2M revenue globally), your Catalyst license can be renewed for free. When you graduate beyond the criteria (e.g., raising Series B, scaling past revenue thresholds, or opening multiple manufacturing plants), you can transition smoothly into our standard predictable enterprise site license.
How is the system deployed and where is our data hosted?
Novaqis is 100% data-sovereign. You can deploy Novaqis on your own facility network / private plant server or in your own private cloud (AWS, Azure, Google Cloud) completely free of infrastructure charges from us. Alternatively, if you do not have an in-house IT team, Novaqis can provide managed private cloud hosting for a modest infrastructure pass-through cost.
Are Computerized System Validation (CSV / GAMP 5) documents included?
The Novaqis software platform includes our built-in Autonomous Validation Engine and automated CSA qualification probes out of the box, generating live verification telemetry and protocol evidence. For facilities requiring custom validation consulting, tailored protocol drafting, onsite qualification execution, or specialized CSV professional services, these human engineering engagements are scoped separately with your regulatory and QA leadership.
How many users and sites can we onboard under the Catalyst grant?
The standard Catalyst grant covers up to 30 named users and 1 manufacturing or testing facility. Because Novaqis never charges per-user seat penalties, you can freely allocate accounts across QA, QC analysts, production supervisors, and IT administrators.
Can we migrate our existing paper STPs, SOPs, and spreadsheets into Novaqis?
Yes. Novaqis Lab Digitize and Novaqis DMS feature automated ingestion tools that convert legacy paper Standard Testing Procedures (STPs), specifications, and document packets into dynamic, electronic worksheets and controlled documents with human-in-the-loop review.
Have specific questions about your manufacturing facility or inspection timelines?
Speak directly with a GxP Software Architect