CIP/SIP process equipment, bioreactors and aseptic filling systems requiring documented FDA/USP Class VI compliant sealing.
Send Your Application DetailsPharmaceutical and biotech equipment must survive repeated Clean-in-Place and Steam-in-Place cycles while proving — with documentation — that the seal will not contaminate the product. A seal that merely survives the cleaning cycle without compliance documentation is not usable in a validated GMP process.
Platinum-cured, FDA and USP Class VI compliant sealing for regulated environments.
View Pharma Silicone →Fluoroelastomer chemical resistance with documented food and pharma compliance.
View FDA/USP FKM →Send your service conditions and required certification — FITCO will recommend a suitable material.
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