Zero tolerance for contamination
Pharmaceutical and wellbeing manufacturing demands the highest material purity, complete traceability, and absolute reliability. We engineer seals to meet those standards.
Pharmaceutical manufacturing leaves no room for error
Material Purity
Every seal material must be fully characterised and traceable. USP-compliant and pharmaceutical-grade polymers ensure no extractable or leachable substances compromise your product.
Sterilisation Resistance
Repeated SIP (steam-in-place) and CIP (clean-in-place) cycles degrade standard seals rapidly. We specify materials that maintain their sealing properties through hundreds of sterilisation cycles.
Regulatory Compliance
Full documentation, batch traceability, and material certificates are standard with every order. We understand the regulatory framework and supply the documentation your quality team requires.
Pharmaceutical sealing applications
Sterile Processing
Tablet Presses
Filling & Capping
Mixing Vessels
Cleanroom Equipment
Wellbeing Products
Transfer Systems
Custom Solutions
Materials and documentation that meet your quality requirements
USP Class VI
Materials meeting United States Pharmacopeia Class VI requirements for pharmaceutical and medical applications.
FDA Compliance
Materials meeting US FDA requirements for food and drug contact. Relevant for manufacturers exporting to the US market.
Full Batch Traceability
Material certificates, declarations of conformity, and batch traceability from raw material to finished seal, supplied as standard.