FDA-grade decontamination protocols for regulated labs. Documented, verified, and audit-ready.
Medical Facility
cGMP environments require validated cleaning procedures — meaning every step is documented, every chemical is tracked, and every surface is verified clean. XIRI provides this level of documentation automatically, so your quality team can focus on science, not janitorial oversight.
We maintain chain-of-custody records for all cleaning chemicals, validated procedure logs, equipment cleaning verification, and cross-contamination prevention documentation. All records are digital, searchable, and audit-ready.
Validated cleaning procedures with documented efficacy
21 CFR Part 211
Chain-of-custody for cleaning chemicals
cGMP
Equipment cleaning verification logs
FDA Guidance
Cross-contamination prevention protocols
21 CFR 211.176
Yes. Our procedures follow cGMP validation requirements with documented efficacy testing, SOPs, and deviation reporting.
Yes. Every chemical used is tracked from receipt through use, with lot numbers, SDS sheets, and usage logs maintained digitally.
Book a free site audit. We'll assess your facility and build a compliance-ready cleaning protocol.
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