PHARMACEUTICAL & BIOTECH
Pharmaceutical and biotech manufacturing demands the highest standards of cleanliness and material purity. SuperKlean stainless steel washdown stations are NSF-certified and designed to meet cGMP requirements for high-purity production environments.
PHARMACEUTICAL WASHDOWN REQUIREMENTS
Material Purity
Pharmaceutical environments require 304 or 316L stainless steel for all product-contact surfaces. Brass and bronze are not acceptable due to potential leaching of copper and zinc into product streams.
NSF/cGMP Compliance
FDA-regulated facilities must use equipment that meets NSF/ANSI standards and is compatible with current Good Manufacturing Practice (cGMP) documentation requirements.
Biofilm Prevention
Smooth, crevice-free stainless steel surfaces resist biofilm formation. SuperKlean stainless models are designed with minimal dead legs and smooth internal surfaces.
Validation Documentation
Pharmaceutical facilities require equipment documentation for IQ/OQ/PQ validation. Northeast Controls provides full technical documentation for all SuperKlean stainless models.
RECOMMENDED FOR PHARMACEUTICAL
NSF-certified stainless steel models designed for high-purity manufacturing environments.
Model 3600M-S
Full 304 stainless steel construction. NSF-certified for food and pharmaceutical contact. Ideal for facilities with hot water supply.
VIEW PRODUCTDuraMix 8000GM-S
NSF-compliant stainless steel steam mixer. Zero steam leak design for pharmaceutical plants with steam supply lines.
VIEW PRODUCTNEED NSF-CERTIFIED WASHDOWN EQUIPMENT?
Our engineers can help you select and document the right stainless steel washdown system for your facility.