XIRI Facility SolutionscGMP Laboratory Decontamination Services
FDA-grade decontamination protocols for regulated labs. Documented, verified, and audit-ready.
Corporate Office
Nightly Commercial Cleaning
cGMP Cleaning Is Not Regular Cleaning
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.
Documentation That Satisfies the FDA
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.
Compliance Checklist
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
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Frequently Asked Questions
Are your decontamination procedures validated?
Yes. Our procedures follow cGMP validation requirements with documented efficacy testing, SOPs, and deviation reporting.
Do you maintain chain-of-custody for chemicals?
Yes. Every chemical used is tracked from receipt through use, with lot numbers, SDS sheets, and usage logs maintained digitally.
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