Launched on India's 80th Independence Day
Make in India for Manufacturers
We built BharatLIMS to take India's labs to the next level. Agentic AI in the workflow. A human signature on every report. Our strength behind every manufacturer, exporter, farmer and producer taking Indian quality to the world.
Request access is for teams already running on BHARATLIMS.AI.
Built for
- NABL / ISO 17025
- FSSAI
- CDSCO
- 21 CFR Part 11
- ALCOA+
The launch moment
Every era of quality begins with a signature.
BHARATLIMS.AI
Chairman · Launched BharatLIMS on India's 80th Independence Day · 15 August 2026
The launch · 15 August 2026
India's labs, ready for Viksit Bharat 2047
As India celebrates its 80th Independence Day, the Prime Minister's vision of a Viksit Bharat by 2047 calls on all of us to take the country's manufacturing and exports to the next level. The free trade agreements now in place give Indian businesses access to global markets, and earning that access means stepping up quality at every stage of manufacturing, from procurement to the final product going out.
Testing laboratories carry that chain of quality. On 15 August 2026, our Chairman, Shri Vijay Kumar Arora, launched BharatLIMS for our group laboratories, making them the first labs in India to embrace artificial intelligence in their operations. The goal is simple: the businesses they serve should always hold results that meet global standards.
BharatLIMS is a laboratory information management system and quality management system in one, built so a lab can scale its capacity and capability in step with the rapid growth of India's manufacturing sector. We believe it will help the labs of our country move to the next level of automation and efficiency, cutting turnaround times and raising the quality of every report.
The .AI in BharatLIMS
Agentic AI in the workflow. A human on every approval.
Agentic and generative AI tools work inside your lab's own data, reading, drafting and flagging around the clock. What they never do is sign: final review and approval always belong to a person.
> which pending samples breach TAT tomorrow?
4 samples across Food & Water. 2 are waiting on HPLC review, 1 on a reagent lot, 1 unassigned.
Showing the unassigned one first.
Ask your lab anything
Plain-language questions over live lab data. “Which pending samples breach TAT tomorrow?” returns an answer, not a report request.
Anomaly detection on results
Trends, drifts and outliers surfaced against historical baselines before they become an OOS investigation.
Turnaround prediction
Realistic completion dates per sample, based on your actual throughput and current queue depth.
Drafted investigations
When a result goes out of specification, the deviation record arrives pre-populated with the relevant history.
Human in the loop, always
AI drafts, suggests and flags. A named, accountable person gives every final review and approval, as international standards require. Nothing reaches a client without a human signature.
Confidential by design
Your lab's data stays your lab's data. The AI tools run against your own instance and your own records, never anyone else's.
Accountable on the record
AI-assisted work lands in the same append-only audit trail as everything else, so responsibility for every report stays complete and unambiguous.
Why labs switch
What you stop worrying about
Not a feature list. These are the questions a lab owner, a quality head and a client-facing manager each lose time to every week.
- 01
Every action on the record
Nothing is deleted, only superseded · Signatures bound to the result they approve
- 02
Role-based access
Granular to the individual action, not just the module · Two-level analyst to reviewer workflow before release
- 03
Nothing goes unbilled
Invoices raised from the booked test list · Rate-card driven pricing, GST-ready
- 04
On time, every time
Deadline tracked per sample · Blockers named, so a delay has an owner
- 05
Light and dark
The most common cause of a failed rollout is analysts working around the software
Every action on the record
An append-only trail carrying user, timestamp and reason. No registers to hunt through when someone asks how you got a number.
- 14:02:11r.deshpandeResult entered
- 14:06:40r.deshpandeSubmitted
- 15:19:03s.iyerReviewedwithin spec
- 15:22:58s.iyerSignedreleased
Role-based access
Authority attaches to roles rather than to whoever happens to know the process, and every access is recorded, not only every change.
| Role | Enter | Review | Sign |
|---|---|---|---|
| Analyst | allow | deny | deny |
| Reviewer | deny | allow | deny |
| Signatory | deny | allow | allow |
Nothing goes unbilled
The tests you ran and the tests you invoiced are the same list, reconciled without anyone checking by hand.
| Sample | Booked | Invoiced |
|---|---|---|
| FBD-24-0917 | ₹4,200 | ₹4,200 |
| FBD-24-0918 | ₹2,800 | ₹2,800 |
| PHM-24-0421 | ₹9,600 | ₹9,600 |
| Unbilled | ₹16,600 | ₹0 |
On time, every time
See which samples are about to miss their deadline, and what is holding them up, before the client calls to ask.
- FBD-24-0917Due todayOn track
- WTR-24-1102Overdue 1dWaiting: reagent lot
- FBD-24-0918Due tomorrowWaiting: HPLC review
- PHM-24-0421Due in 3dOn track
Light and dark
Long shifts, dim instrument rooms and night shifts are real. Pick what suits the bench and the system remembers it.
Every action on the record
An append-only trail carrying user, timestamp and reason. No registers to hunt through when someone asks how you got a number.
- 14:02:11r.deshpandeResult entered
- 14:06:40r.deshpandeSubmitted
- 15:19:03s.iyerReviewedwithin spec
- 15:22:58s.iyerSignedreleased
Role-based access
Authority attaches to roles rather than to whoever happens to know the process, and every access is recorded, not only every change.
| Role | Enter | Review | Sign |
|---|---|---|---|
| Analyst | allow | deny | deny |
| Reviewer | deny | allow | deny |
| Signatory | deny | allow | allow |
Nothing goes unbilled
The tests you ran and the tests you invoiced are the same list, reconciled without anyone checking by hand.
| Sample | Booked | Invoiced |
|---|---|---|
| FBD-24-0917 | ₹4,200 | ₹4,200 |
| FBD-24-0918 | ₹2,800 | ₹2,800 |
| PHM-24-0421 | ₹9,600 | ₹9,600 |
| Unbilled | ₹16,600 | ₹0 |
On time, every time
See which samples are about to miss their deadline, and what is holding them up, before the client calls to ask.
- FBD-24-0917Due todayOn track
- WTR-24-1102Overdue 1dWaiting: reagent lot
- FBD-24-0918Due tomorrowWaiting: HPLC review
- PHM-24-0421Due in 3dOn track
Light and dark
Long shifts, dim instrument rooms and night shifts are real. Pick what suits the bench and the system remembers it.
Panels are illustrative of the interface. Sample identifiers and figures are examples, not customer data.
Modules
Seven modules. One database. No seams.
Each module is the system of record for its stage of the lifecycle, and every one of them writes to the same audit trail.
Every sample, tracked from the front door
A sample becomes a record the second it arrives, and never stops being one.
- Instant registration with a unique ID and barcode on arrival
- Live chain of custody from reception to disposal
- Client, batch and matrix captured in a single screen
- Real-time status visible to the whole lab
Book it once. Everything follows
One booking drives labels, pricing, routing and the analyst's worksheet.
- Auto-generated barcodes and labels per sample and aliquot
- Rate-card driven pricing, quotations and approvals
- Automatic department and section allotment
- Test and parameter selection from your method library
From instrument to record, automatically
Readings land in the worksheet untouched by hand. No transcription, no drift.
- Direct data capture from HPLC, GC, ICP, balances and more
- Method-linked worksheets with validated calculations
- Specification limits with automatic OOS and OOT flagging
- Raw data retained and re-inspectable for every result
Reviewed, signed, defensible
Two pairs of eyes, one signature, and a record that stands up in an audit.
- Two-level analyst to reviewer workflow
- 21 CFR Part 11-style electronic signatures
- Certificate of Analysis generated on release
- Nothing leaves the lab until it is signed
Quality built in, not bolted on
The quality system lives in the same database as the results it governs.
- CAPA, deviations and OOS investigations
- Document and SOP control with revision history
- Training records mapped to methods and personnel
- Internal audit planning and closure tracking
Never run dry mid-batch
Reagents, standards and consumables tracked down to the lot and the test.
- Reagent and standard tracking with lot and expiry
- Consumption recorded per test, not per guess
- Low-stock and expiry alerts before they bite
- Full traceability from lot to reported result
Reported and invoiced in one flow
The tests you booked are the tests you bill, reconciled automatically.
- Auto-invoice generated from the booked test list
- GST-ready billing and documentation
- Client ledgers with outstanding and ageing
- Export to your accounting system
Compliance
Written for the audits you actually face
BharatLIMS.AI is built around Indian regulatory practice first, with the international frameworks your clients ask about layered on top.
- NABLISO/IEC 17025
Method validation records, traceability of measurement and competence records structured the way assessors expect.
- FSSAIFood safety
Food matrix templates, statutory parameter sets and report formats for notified laboratories.
- CDSCOPharmaceutical
GLP and GMP aligned workflows, specification control and batch release documentation.
- 21 CFR 11Electronic records
Unique user identity, electronic signature meaning, and an audit trail that cannot be switched off.
- ALCOA+Data integrity
Attributable, legible, contemporaneous, original and accurate, enforced by the data model rather than by policy.
Validation is a shared exercise: we supply qualification documentation, traceability matrices and audit-trail exports; your quality team owns the validated state of the installed system.
FAQ
The questions labs actually ask
Something not covered here? Ask it directly on the demo call. We’d rather answer it properly than in a footnote.
Can BharatLIMS.AI be validated for a NABL or ISO 17025 assessment?
Does it support 21 CFR Part 11 electronic signatures?
Which instruments can you connect?
Can we run it on our own servers?
How long does implementation take?
Can one instance handle multiple labs or locations?
How is our data secured?
Request a demo
See it run on your lab’s own workflow
Tell us a little about your lab and we’ll come to the call prepared, with your matrix, your volumes and your compliance obligations already in mind.
45 minutes, no slides
We open the system and run your workflow. If we can't show it, we'll say so.
Your sample, your report
Bring a real sample journey and a report format you already issue. We'll model it live.
The audit trail, in full
We'll pull the audit trail on a result and export it exactly as an assessor would ask for it.
A straight answer on fit
If BharatLIMS.AI isn't right for your lab, we'll tell you on the call rather than after a pilot.
Prefer email? Write to info@bharatlims.ai