Rooms
High-assurance room decontamination with VH₂O₂ technology
Controlling microbial contamination in GMP production rooms
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