Medical Device Cleaning Validation
Reusable medical devices require documented cleaning validation to prevent cross-contamination and meet FDA, ISO, and EU MDR expectations.
Reusable medical devices require documented cleaning validation to prevent cross-contamination and meet FDA, ISO, and EU MDR expectations. Medical Device Cleaning Validation - Microchem Laboratory designs and executes custom studies that replicate real-world use including soil load application, simulated use cycles, and cleaning procedure analysis. We evaluate residue levels and cleaning efficacy using validated recovery methods, then provide full reporting to support regulatory filings and IFUs. Our team works directly with quality engineers and regulatory staff to ensure your cleaning process is efficient, reproducible, and fully documented.
