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Pharmaceutical & Biotech
Aseptic manufacturing demands absolute sterility assurance. Our vH₂O₂ generators achieve 6-log10 microbial reduction across pass boxes, cRABS, isolators, filling lines, and entire cleanroom suites.
No dehumidification pre-phase means faster cycles and more batches per shift. Use any Food grade H₂O₂ (35–50%) — no proprietary consumables.
Frequently Asked Questions
Is DECX validated for ISO 5 / Grade A aseptic environments?
Yes. DECX vH₂O₂ systems are deployed in aseptic manufacturing, cRABS, isolators, and pass boxes to achieve 6-log₁₀ sterility assurance in ISO 5 / Grade A cleanrooms.
What pharmaceutical regulators recognise the deployments?
WHO GMP, NABH, JCI, and FSSAI alignment is built into the IQ/OQ/PQ documentation and bioindicator-test workflow.


