Swat iQua SuiteIndia
Pharma quality software for India — built in Rajkot, ready for Schedule M.
From MSME plants to multi-site groups, Indian manufacturers face Revised Schedule M at home and FDA, MHRA or WHO inspections abroad. Swat iQua Suite puts LIMS, QMS, eBMR and materials on one audit trail for both.
- Built and supported in India
- Revised Schedule M readiness
- Same records for export inspections
- Pay only for live modules
Your regulators
Designed for the rules you are inspected against.
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Revised Schedule M
India’s updated GMP, now enforced through risk-based inspections by state licensing authorities.
Schedule M hub -
WHO GMP & export markets
WHO GMP for many export markets, plus US FDA and EU expectations if you supply them.
WHO GMP -
Data integrity
ALCOA+ records, audit trails and electronic signatures — expected by CDSCO and export inspectors alike.
ALCOA+
Start where it hurts
Free Schedule M tools for Indian plants.
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Readiness assessment
25 questions, an instant score and a full gap report by email.
Start the assessment -
Gap checklist
Walk your site area by area — Word and PDF.
Get the checklist -
ROI in rupees
Estimate what paper batch records and audit prep cost you, in INR.
Open the calculator
Customer stories
From Indian API plants to UK laboratories.
“Ten years on, we would choose it again.”
We moved our QC LIMS onto SwatTech in 2016 and have never looked back. Every specification, result and calibration is one search away, and every change explains itself. When inspectors arrive, we don’t prepare — we simply open the system.
“Audits are something we welcome now.”
In contract testing, our reputation rides on every result we sign. A second-person review on every result, a complete audit trail and a client portal that delivers reports and CoAs on time have turned audits from something we braced for into something we welcome.
“Any batch, traced in one click.”
In API manufacturing, traceability is everything. Today we follow any batch back to its raw-material lots and forward to every shipment in seconds. Revised Schedule M no longer feels like a deadline — it feels like the way we already work.
Delivered remotely
How we take you live from India.
Our team in Rajkot implements Swat iQua Suite remotely, in your working hours where they overlap with ours — the same way we have supported UK laboratories since 2016.
- 01
Online workshops
We map your processes, roles and records with your team over video calls.
- 02
Configuration
Sites, users, workflows, masters and signatures set up for your organisation.
- 03
Data migration
Legacy records mapped, trial-loaded, reviewed by you and reconciled.
- 04
Validation & training
Requirements traceability, Part 11 controls evidence and role-based training.
- 05
Go-live & support
Typical go-live in 1–3 months, then direct support from the team that builds the product.
Talk to us
Our hours, in your time zone.
One team, based in Rajkot, India. Where our hours do not overlap with yours, book a call at a time that suits you.
- India
- 09:30 – 19:00 ISTMon–Sat · Our office hours
- United Kingdom
- 09:00 – 13:30 GMTMon–Fri · Live calls, your local time
- UAE & Gulf
- 08:00 – 17:30 GSTMon–Fri · Live calls, your local time
Book a demo at a time that suits you WhatsApp us (opens in a new tab)
FAQ
Frequently asked questions
Can’t find your answer? Talk to our team — we reply within one business day.
Is Swat iQua Suite suitable for MSME manufacturers?
Yes. Licensing is modular, so a smaller plant can start with the quality system or the QC lab and add modules and sites as it grows.
Can we meet Revised Schedule M and export requirements with one system?
Yes. The same records serve CDSCO inspections and export inspections — Swat iQua Suite is designed to comply with Revised Schedule M, 21 CFR Part 11, EU GMP Annex 11 and WHO GMP.
Where is your team?
In Rajkot, Gujarat. Call +91 95107 17999 or +91 99131 56229, WhatsApp us, or visit our office.
Ready to see Swat iQua Suite in action?
Book a free, personalised demo and see how Swat iQua Suite takes your plants, labs and quality teams from paper to inspection-ready.