Rooms

High-assurance room decontamination with VH₂O₂ technology

Controlling microbial contamination in GMP production rooms

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Description

Controlling microbial contamination in GMP production rooms, R&D animal facilities and hospital environments is a continuous challenge. High ceilings, dense equipment layouts, hidden surfaces and sensitive electronics make manual wiping both impractical and unreliable. Operator-dependent techniques lead to inconsistent pressure, variable contact time and non-uniform application. This makes reproducibility difficult to achieve and validation even harder.

Airborne VH₂O₂ decontamination overcomes these structural limitations. Dry-fog atomization reaches elevated, obstructed and inaccessible surfaces with no operator dependency, ensuring homogeneous distribution throughout the entire room. Cycles are fully traceable, predictable (21 CFR Part 11) and validated according to EN 17272, guaranteeing real 6-log microbial reduction.

Hydrogen peroxide at moderate concentration provides powerful disinfection while preserving materials; it naturally decomposes into water and oxygen, leaving no residues and ensuring compatibility with sensitive equipment.

For routine sanitation, batch changeover or preventive environmental control, airborne VH₂O₂ decontamination is the most reliable way to achieve high-level microbiological assurance in complex room configurations.

Quality & Compliance

All Solidfog equipment complies with the highest international quality standards :

Key features

ISO 9001:2015

Certified Quality Management System

EN 17272:2020

Validated efficacy for automated airborne surface disinfection

CE Marking

Full compliance with European directives

Data integrity

Audit trail and 21 CFR Part 11 complianceAudit trail and 21 CFR Part 11 compliance

GMP Design

Fully aligned with pharmaceutical industry requirements

Qualification protocols

DQ, FAT, SAT, IQ/OQ available

Calibration certificates

Supplied for all critical component