Industry 02
Pharmaceutical Industries
In pharmaceutical manufacturing, zero contamination is non-negotiable. Trinity Valves supplies hygienic, sanitary-grade valves with zero dead-leg design, Ra ≤ 0.4 µm internal surface finish, and full compliance with FDA 21 CFR and cGMP requirements — protecting product purity from API synthesis through final fill.
FDA Compliant
GMP Grade
Sanitary
SS 316L
CIP/SIP Ready
Hygienic Design
- Zero dead-leg configuration
- Ra ≤ 0.4 µm (electropolished)
- Crevice-free body geometry
- Full-bore flow path
Certifications
- FDA 21 CFR Part 11
- cGMP / GEP compliant
- EHEDG certified
- 3-A Sanitary Standards
Process Compatibility
- WFI & purified water
- Steam-in-place (SIP)
- Clean-in-place (CIP)
- Sterile gas & solvent service
Technical Specifications
| Parameter | Details |
|---|---|
| Size Range | ¼" to 12" (DN8–DN300) |
| Material | SS 316L / SS 304L |
| Surface Finish | Ra ≤ 0.4 µm (electropolished) |
| Connections | Tri-Clamp / DIN / SMS / Butt Weld |
| Temp Range | −20°C to +140°C (SIP up to 160°C) |
| Testing | Hydrostatic, Helium Leak, Biocompatibility |
Valve Types Supplied
Aseptic Diaphragm Valves
Sanitary Ball Valves
Butterfly Valves (Tri-Clamp)
Sampling Valves
Pressure Relief Valves
Typical Applications
API manufacturing, biofermentation, water-for-injection (WFI) systems, CIP/SIP skids, vaccine production, and sterile fill-finish lines.
