Nine paying clients across India and the US. Four products in active deployment: document search, AI compliance agents, knowledge systems, and sales intelligence.
Built for the compliance, regulatory, and commercial challenges that organisations are paying to solve today.
Make every compliance document, SOP, batch record, and regulatory filing instantly queryable, so your teams stop spending hours searching and start finding answers in seconds.
Deploy AI agents across your electronic Trial Master File to surface the most relevant findings for QC audits, without your team manually reviewing hundreds of documents.
A 21 CFR Part 11 compliant ELN built for pharmaceutical R&D and manufacturing, with the data integrity controls regulators expect and the usability scientists actually want.
Give your commercial team better routing, smarter physician recommendations, and automated follow-up, so reps spend their time on the right contacts and nothing falls through the cracks.
The same AI infrastructure, purpose-configured for how your industry actually operates.
Compliance search, eTMF agents, lab notebooks, and sales intelligence for CDMOs, generics manufacturers, and pharma commercial teams. Nine paying clients across India and the US. 21 CFR Part 11 compliant.
See pharma solutions →OCR invoice extraction, TDS automation, payroll conversion, P&L risk flagging, VAT/CT compliance workflows, and IFRS audit reporting. Built for CA firms and accounting consultancies across India and the UAE.
Smarter territory routing, automatic call summaries, follow-up automation, and payment reminder systems so teams spend time on the right accounts and nothing falls through the cracks.
UAE VAT and Corporate Tax registration workflows, FTA compliance calendars, and IFRS audit reporting suites. Built for regulated businesses that need structured, auditable outputs.
Custom learning applications with content delivery, progress tracking, and assessment functionality. Built for training organisations and education NGOs deploying at scale.
We start with two completely free steps so you know exactly what you're getting before committing a dollar.
We run a hands-on session with your team to identify high-value AI use cases in your organization. No sales pitch. Just strategic insights.
100% FreeWe deliver a strategic deck with prioritized recommendations, ROI estimates, and implementation timelines. Yours to keep, no strings attached.
100% FreeIf you choose to proceed, we build the solution ourselves, or connect you with specialized partners for niche use cases. You're in control.
Your DecisionBook your free workshop today. No commitment. No cost. Just clarity on what AI can do for your business.
How a leading Indian CDMO gave its formulation scientists the ability to search a decade of proprietary data in seconds
Encube Ethicals had accumulated over a decade of proprietary R&D data: formulation studies, stability reports, excipient compatibility data, clinical batch records, and regulatory submissions. This knowledge lived across shared drives, lab notebooks, and disconnected document management systems.
When formulation scientists began new drug development projects, they had no reliable way to query what the organization already knew. Teams were unknowingly duplicating studies, starting formulations from scratch when relevant historical data existed, and losing weeks to knowledge retrieval that should have taken minutes.
"We had years of formulation and compliance data that was effectively invisible to our teams. Livo built something that made all of it searchable in a way our scientists actually use every day."
"We had years of formulation and compliance data that was effectively invisible to our teams. Livo built something that made all of it searchable in a way our scientists actually use every day."
"The eTMF review work that used to take our team days to prepare now gets surfaced in a fraction of the time. Livo's agents understand what matters in a regulatory context."
"Our reps are spending more time on the right physicians and less time on admin. The automated follow-up alone has changed how our field team operates."
"We needed better visibility into how our commercial team was spending their time and whether it was translating into the right outcomes. Livo gave us that, and then some."
Every project starts with understanding your specific workflow. We scope, build, and deploy from there — no templates, no guessing.
On-premise semantic search over a decade of proprietary R&D data — formulation records, stability studies, batch records, and regulatory filings — making institutional knowledge instantly queryable.
Full-stack platform for a Dubai accounting consultancy: OCR document processing, UAE payroll with SIF generation, VAT and Corporate Tax registration workflows, IFRS audit reporting, management dashboards, CRM, and client portal.
AI automation for a Bangalore CA firm: TDS challan extraction from the Income Tax portal, invoice OCR, payroll data conversion, P&L entry risk categorization, and Zoho Books integration for sales and purchase registers.
Automated WhatsApp and email payment reminder system with a report generation bot, reducing manual follow-up and giving the team structured visibility into outstanding payments.
Mobile English learning application for one of India's largest education NGOs, with structured content delivery, progress tracking, and assessment functionality.
Why pay six figures for discovery when you can get it free?
Start with zero risk. Get professional insights and a custom roadmap before spending a dollar.
Not another API wrapper. Real systems built for scale, security, and accuracy.
Your data stays in your infrastructure. Full control over deployment environment and data residency.
Data processing and storage of Indian citizens on India servers. Full compliance with Digital Personal Data Protection regulations.
We build systems that meet GDPR requirements. Data privacy and protection by design.
Specific answers to the questions pharmaceutical teams, CDMOs, and enterprise leaders ask when evaluating AI systems.
Most pharma document search pilots go live in 4–6 weeks — covering ingestion of SOPs, batch records, regulatory filings, and stability studies, plus a semantic search layer your teams can query in natural language. Full enterprise rollouts with role-based access and DMS integration typically take 2–3 months.
The highest-ROI applications are: (1) semantic search across formulation records so scientists find historical work in seconds, not days; (2) automated eTMF review to surface audit-relevant findings before inspections; (3) 21 CFR Part 11-compliant electronic lab notebooks. Companies using AI for knowledge retrieval report significant drops in duplicated studies and formulation rework.
Yes. AI agents can be deployed across an electronic Trial Master File to identify audit-relevant findings, flag missing documents, and organise outputs by document type and risk level — reducing manual QC prep from days to a fraction of the time.
Part 11 compliance requires electronic signatures, complete audit trails, and access controls built into the system from day one — not bolted on after. Every data entry, edit, and signature event must be logged with a time-stamped, attributable record. We build these controls into the core of every system we deploy.
Yes — and for most CDMOs and manufacturers this is non-negotiable. We deploy all AI systems within your own infrastructure. No proprietary formulation data, batch records, or regulatory filings are ever sent to external servers or third-party APIs. Sensitive client data stays siloed by design.
Three ways: (1) territory routing that prioritises physicians by prescribing patterns, (2) automatic call summarisation so reps skip post-call admin, and (3) automated follow-up and next-best-action recommendations. Teams using AI-assisted rep intelligence report significantly more time spent on the right contacts.
For a typical pharma corpus — formulation records, stability studies, batch records, and regulatory filings accumulated over a decade — ingestion and indexing takes days to a few weeks depending on volume and format. Once deployed, queries across the full corpus return results in seconds.
A pilot scopes one use case — for example, semantic search across one product line's formulation records — and can go live in 4–6 weeks. A full enterprise deployment covers your entire corpus, integrates with LIMS, DMS, and ERP systems, implements role-based access, and takes 3–5 months. Most companies start with a pilot to validate ROI before scaling.
Co-Founder
Ex-McKinsey
IIM-Ahmedabad
IIT-Delhi, Computer Science
Co-Founder
Ex-McKinsey
IIM-Ahmedabad
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