IndustriesBy plant · by role
Pharma software for every plant and every quality role.
Swat iQua Suite is one platform, but an API plant, a tablet line, an aseptic filling suite and a contract testing lab each lean on different parts of it. Start with the page that looks most like your site — or with the role you hold.
- API, oral solid dosage and sterile plants
- CDMOs and contract testing labs
- Pages for QA, QC, production and IT/CSV leads
By plant
Built around how your site actually makes and tests medicines.
Every industry page shows the records, gates and hand-offs Swat iQua Suite enforces for that kind of operation — on the same audit trail, users and e-signatures as the rest of the platform.
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API manufacturing
Intermediate control, a single reuse gate for recovered solvents and materials, mass balance and lot genealogy on the eBMR engine.
API manufacturing software -
Oral solid dosage
Approved formulas, verified dispensing, step-by-step batch records, printed-component reconciliation and in-house QC for tablets and capsules.
OSD manufacturing software -
Sterile injectables
Gowning, cleanroom, EM and media-fill gates on aseptic steps, plus sterilisation, lyophilisation, CCIT and visual inspection.
Sterile injectables software -
CDMO & contract manufacturing
Multi-company, multi-site control with shared or site-owned masters, client-specific specifications and a client portal.
CDMO software -
QC testing labs
Sample management, controlled result import, second-person review, client portal and CoA dispatch for contract and in-house labs.
QC laboratory software
By role
What’s in it for you.
The same records, seen from the desk of the person accountable for them.
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QA heads
Every deviation, CAPA and change linked, tracked and closed on time, with a full audit trail.
For QA heads -
QC managers
Specifications, testing, stability and instruments in one place; results reviewed before they count.
For QC managers -
Production heads
Guided batch execution, verified dispensing and fewer batch-record errors.
For production heads -
IT & CSV teams
One system to validate, with MFA, role-based access, a complete audit trail and secure cloud hosting.
For IT & CSV teams
Customer stories
QC labs and API manufacturers already work this way.
“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.
FAQ
Frequently asked questions
Can’t find your answer? Talk to our team — we reply within one business day.
Is there a separate product for each industry?
No. Swat iQua Suite is one platform with 85+ integrated modules. Each site switches on the modules it needs — sterile modules, for example, only appear at sites where the sterile feature is enabled.
Can one installation cover an API plant, a formulation plant and a QC lab?
Yes. Swat iQua Suite is multi-company and multi-site: each record belongs to a site, master data can be shared globally, with chosen sites or kept site-owned, and each site can run a different manufacturing configuration.
We only need a QC lab system today. Is that possible?
Yes. Licensing is modular, so you pay for the modules active in your current phase. Many customers start with the quality foundation or the QC laboratory and add manufacturing later.
Which regulations is Swat iQua Suite designed for?
Swat iQua Suite is designed to comply with 21 CFR Part 11, EU GMP Annex 11 and Annex 1, WHO GMP and Revised Schedule M, following ALCOA+ data-integrity principles and a GAMP 5 risk-based validation approach.
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.