PHARMA · LIMS · QMS · ERP

Pharma software — compliant labs & API manufacturing.

Compliance-first software for the pharmaceutical industry: iQuaLiMS for laboratory and quality management, and PharmaAPI ERP for active pharmaceutical ingredient manufacturing — validated to 21 CFR Part 11, EU Annex 11 and ALCOA+.

Validated toCompliance
  • 21 CFR Part 11
  • ALCOA+
  • GAMP 5
Pharma Software

Regulatory-grade by design

Pharma software cannot cut corners. Every workflow we build carries traceability, electronic signatures and audit trails aligned with 21 CFR Part 11, EU Annex 11, Schedule M and ALCOA+ principles.

From the QC lab to API production, our platforms replace paper with validated, inspection-ready digital records.

  • 21 CFR Part 11 & EU Annex 11 aligned
  • ALCOA+ data integrity
  • GAMP 5 validated approach
  • Cloud-based, inspection-ready
PHARMA · LIMS · QMS · ERP
Seamless. Paperless. Stressless.
LIMSeQMSCAPACPMSAPI ERPInstruments
Capabilities

Our pharma platforms

Two products covering the lab and the plant.

01

iQuaLiMS — LIMS

Sample & batch management, OOS investigations and specifications.

02

eQMS

Change control, CAPA, incidents and document management.

03

CPMS & Instruments

Calibration, preventive maintenance and instrument integration.

04

LMS & UAM

Training, certification and granular user access management.

05

PharmaAPI ERP

Batch production, procurement and dispatch for API manufacturing.

06

Analytics

Dashboards for usage, sample analysis and compliance.

Why Swat Info System
Compliance and clarity in one ecosystem.
21 CFR Part 11ALCOA+GAMP 5
The outcome

Outcomes for pharma companies

  • Inspection-ready records at any moment
  • Consolidated QMS, LIMS and LMS
  • Faster, paperless QC workflows
  • Lower compliance risk and cost
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Related expertise

FAQ

Frequently asked questions

Compliance-first software for the pharmaceutical industry: iQuaLiMS for laboratory and quality management, and PharmaAPI ERP for active pharmaceutical ingredient manufacturing — validated to 21 CFR Part 11, EU Annex 11 and ALCOA+.

Core capabilities include iQuaLiMS — LIMS, eQMS, CPMS & Instruments, LMS & UAM — all in one integrated system.

Yes. We adapt it to your exact workflows and integrate with your existing tools. Inspection-ready records at any moment.

Book a demo and our Rajkot-based team will map Pharma Software to your requirements, then plan a phased rollout with training and support.

Get started

Digitise your pharma quality and production.

Book a walkthrough of iQuaLiMS and PharmaAPI ERP for your facility.