We combine chemical process engineering with electrical control and standardized testing in a six-step workflow designed for GMP-adjacent environments.
We confirm catalyst type, material, and application in a brief technical conversation. You receive a simple intake checklist to guide the scoping step. Screening is free.
On arrival, components are assigned a batch ID, visually inspected, and baseline-tested under defined conditions. Every part is traceable from this point forward.
Controlled oxidative treatment at low temperature and defined relative humidity, followed by temperature-controlled enrichment of the surface. The process is gentle on supports, adhesives, and mechanical structures.
Aeration and conditioning ensure a residue-free end state and stable activity before final testing. This step is a non-negotiable part of every batch we deliver.
Standardized performance measurement and quality control, logged for traceability. Supported by ISO 15202 (ICP-QMS) testing from an accredited third-party laboratory when required.
You receive a before/after report with test conditions, results, and recommendations. Components are shipped back to site. Documentation is structured for QMS storage and can be aligned with your internal formats on request.
We report circular effects at batch level, including share of parts kept in service, waste reduction by mass and material type, and lead-time gains versus new procurement. When requested, we add an LCA-supported estimate of potential CO₂e impact with assumptions clearly stated, so operations, procurement, and sustainability teams can all rely on the same numbers.
Send us a brief description of your catalysts and timeline. We'll reply with an intake checklist and proposed next steps.
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The world's first reactivation service for pharmaceutical-grade H₂O₂ isolator catalysts. Validated, documented, returned in days.
