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Pharma & Medical

Aseptic process measurement meeting hygienic and compliance requirements.

Pharmaceutical manufacturing has explicit requirements for hygienic rating, cleanability and material compliance. Wetted parts should be flush-diaphragm or fully welded with no cleaning-resistant crevices, satisfying CIP/SIP requirements.

Electropolishing wetted surfaces to Ra ≤ 0.4 μm inhibits microbial adhesion; Tri-Clamp connections allow fast removal. Sanitary pressure transmitters and radar meters serve fermenters and compounding tanks; multi-point RTDs validate steriliser temperature.

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