Orchestrating efficient laboratory operations.
Unify sampling, testing, stability, calibration, inventory and microbiology in one platform — with audit-ready compliance built in from day one.
- 21 CFR Part 11 ready
- ALCOA+ aligned
- GAMP 5 categorised
- ISO/IEC 17025 compatible
One platform. Complete control. Unmatched confidence.
Built for QA, QC and lab managers who can’t afford a paper-trail gap, a missed timepoint, or a calibration that slipped past its due date.
Ensure data integrity
Tamper-evident audit trails, e-signatures and version control protect every record from generation to disposal.
Boost operational efficiency
Automate manual tasks, parallelise approvals and cut sample-to-report turnaround from days to hours.
Stay secure & compliant
Role-based access, encrypted storage and pre-mapped controls for 21 CFR Part 11, GxP and ISO 17025.
Make better decisions
Live dashboards, trend analysis and exception alerts turn lab data into operational insight.
Everything your lab does, in one connected system.
Nine deeply integrated modules sharing one data model and one audit trail — built on the same compliance-first foundation.
Sample Management
End-to-end sample lifecycle, from registration to disposal — with complete chain of custody.
Workflows
Define, automate and enforce your lab SOPs — without writing code.
Worksheets
Interactive digital worksheets with built-in calculations and audit trail.
Inventory Management
Working, reference, impurity and primary standards — with shelf-life, usage and chain-of-custody.
Stability Management
Plan, execute and defend your stability programme — protocol to shelf-life.
Calibration Management
One system. Every instrument. Total accuracy.
Microbiology Management
Culture, media, water and environmental monitoring — one connected system.
Instrument Integration
Direct integration with lab instruments — no transcription, no errors.
ERP Integration
Seamless data exchange with SAP, Oracle and other ERPs.
From sample registration to certificate of analysis — without a single paper form.
- 01Sample Management
Register samples with required fields, specs and chain of custody.
- 02Sample Allocation
Assign tests, methods and analysts. Allocate to instruments in seconds.
- 03Test Execution
Capture results directly from instruments. Auto-calculate against limits.
- 04Review & Approval
Parallel/sequential approvals with e-signatures and complete audit trail.
- 05Reports & COA
Generate compliant COAs and regulatory reports with one click.
Audit-ready by default.
LimsPulse maps cleanly onto the standards your auditors check — and supports them across every module.
21 CFR Part 11
Time-stamped audit trails, e-signatures with meaning and signed-record binding for FDA-regulated electronic records.
ALCOA+
Attributable, Legible, Contemporaneous, Original, Accurate — plus Complete, Consistent, Enduring and Available.
GAMP 5
Category 4 configurable product with IQ/OQ templates, risk register and change-control built in.
ISO/IEC 17025
Method validation, calibration traceability, PT/EQA and uncertainty handling as first-class concepts.
The questions we get asked most
Quick answers for QA, QC and IT teams sizing up LimsPulse.
See LimsPulse in your lab.
Walk through your highest-volume workflow with our team. We’ll show you exactly how it runs in LimsPulse.