Cleanroom Validation Services in India
ISO 14644-3 testing with audit-ready reports by our own validation team.
Validation & Services
Cleanroom Validation
Documented qualification of cleanrooms and clean-air equipment for regulatory audits, customer audits and periodic requalification.
Used in pharmaceutical, biotech, hospital, research and electronics cleanrooms.
What is included
- HEPA filter integrity (PAO / DOP) testing
- Non-viable particle counts
- Air velocity, air changes and pressure cascade
- Recovery and airflow visualisation (smoke) studies
- DQ / IQ / OQ / PQ documentation
Why Lab Services
One accountable partner, since 1997
- Single-point responsibilityDesign, manufacturing, installation and validation by one team.
- Made in IndiaBased at GIDC Makarpura, Vadodara, at the heart of India's pharmaceutical belt.
- Compliance by designEngineered around ISO 14644-1, ISO 14644-3, EU GMP Annex 1, WHO GMP requirements.
- ISO 9001 & ISO 45001 certifiedAudit-ready documentation with every project.
Common questions
Frequently asked questions
Where does Lab Services supply cleanroom validation?
Lab Services is based at GIDC Makarpura, Vadodara, Gujarat, and serves clients across India. For projects outside India we supply flat-packed modular systems with complete documentation and installation supervision.
Which standards do you design to?
Our designs and validation follow ISO 14644-1, ISO 14644-3, EU GMP Annex 1, WHO GMP, Revised Schedule M, USFDA cGMP.
How do I get a quotation for cleanroom validation?
Send your URS, layout or required sizes to sales@labservicesindia.com, or call or WhatsApp +91 98250 72978. We usually reply within one working day.
Related products
More from Validation & Services
Need cleanroom validation for your facility?
Share your URS or layout for a detailed proposal.