Pharma QMS & Compliance Automation for India
LImpulse automates your pharma QMS — SOPs, batch records, CAPA, and audit trails — so your next CDSCO inspection is your easiest one yet.
30-day free trial · No credit card · Live in under a week
QMS dashboard
Remidex Pharma · Unit 1
Schedule M compliance
94%
Next audit in
18 days
Open CAPAs
2
SOPs current
34/36
Cal. due
1
The problem
Binders don't pass inspections
Paper-based SOPs go missing, signatures can't be traced, and version history doesn't exist. CDSCO inspectors find gaps in minutes that took months to create.
Excel breaks at audit scale
There's no signature trail, no access control, and no way to prove who changed what and when. Schedule M requires evidence your spreadsheet can't produce.
Inspections arrive without warning
CDSCO risk-based inspections are unannounced. When the team walks in, your QMS either speaks for itself — or it doesn't.
How LImpulse works
Set up in days, not months
Our onboarding team migrates your SOPs, batch records, and CAPA history from Excel and paper into LImpulse. Most teams are fully live within 5–7 working days.
Manage everything in one place
SOPs, batch records, deviations, CAPA, calibrations, audit trails — one platform, one login. Your QA team spends time on quality, not on finding documents.
Walk into any inspection with confidence
Every action is timestamped and attributed. Your Schedule M compliance score updates in real time. When the inspector asks for a record, you pull it up in seconds.
Features
SOP management
Version-controlled SOPs with electronic approval workflows and auto-expiry alerts.
Batch records
Digital batch manufacturing records with real-time fill and electronic signatures.
Deviation logging
Capture deviations at batch level, automatically linked to a CAPA.
CAPA tracking
Assign, track, and close corrective actions with deadline reminders and escalation.
Instrument calibration
Schedule calibrations, receive alerts, maintain a complete calibration history.
Audit trail
Timestamped, tamper-proof trail for every action — inspection-ready by default.
Schedule M checklist
Built-in checklist mapped to every clause of Revised Schedule M.
Role-based access
QA Manager, QC Analyst, Production — each role sees exactly what they need.
Electronic signatures
21 CFR Part 11-aligned e-signatures for records requiring authorised sign-off.
Pricing
All plans include a 30-day free trial. No credit card required.
Starter
₹4,999/month
For single-unit manufacturers starting their QMS journey
✓Up to 5 users
✓SOP management
✓CAPA tracking
✓Batch records
✓Email support
Growth
₹9,999/month
For manufacturers preparing for WHO-GMP or USFDA audits
✓Up to 20 users
✓Everything in Starter
✓Multi-site dashboard
✓Calibration management
✓Schedule M checklist
✓Priority support
Enterprise
Custom
For multi-site operations with complex compliance needs
✓Unlimited users
✓Everything in Growth
✓API access
✓Custom workflows
✓Dedicated QMS consultant
✓SLA support
FAQ
Is your QMS ready?
30-day free trial · No credit card · Live in a week