The Rigorous Requirements for Valves in the Food and Pharmaceutical Industries

The food and pharmaceutical industries have extremely high standards for fluid control equipment. Any contamination can lead to batch spoilage, product recalls, and even endanger patient/consumer safety. The core challenge in this industry lies in…

  • Sterility Assurance: Valves must be free of dead legs to ensure thorough sterilization and prevent microbial contamination.
  • Zero-Residue Verification: Following CIP/SIP cleaning, the process medium must be completely drained to eliminate the risk of cross-contamination between batches.
  • Compliance: All wetted materials must comply with FDA standards, and the equipment must meet cGMP requirements.
  • Traceability: Complete material certificates, surface roughness reports, and validation documentation are required.
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KINKO's Commitment

JINKO possesses a deep understanding of the compliance requirements and process-related pain points inherent to the food and pharmaceutical industries. We not only supply valves that meet FDA and GMP standards, but also leverage our patented zero-residue design to help clients fundamentally eliminate the risk of cross-contamination and successfully pass GMP validation.

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Core Solutions

Precise Dispensing and Mixing
  • Multi-purpose (diverting/combining)
  • Simplifies piping design
  • Saves 30% installation space
Sanitary On/Off & Regulation
  • Quick-release clamp, easy to clean
  • 1-million-cycle service life
  • Class VI zero leakage
Sterile-Grade Fluid Control
  • Zero dead-leg design options
  • FDA/GMP compliant materials
  • CIP/SIP compatible

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FAQ

What certifications and standards do KINKO valves meet for pharmaceutical and food processing applications?
KINKO valves comply with FDA 21 CFR Part 177, EU GMP Annex 1, and 3-A sanitary standards. We provide full material certificates, surface roughness reports (Ra≤0.4μm), and complete validation documentation to support your regulatory compliance.
How does the patented zero-residue design prevent cross-contamination in multi-product pharmaceutical lines?
Our patented zero-dead-leg flow path ensures complete drainage after CIP/SIP cycles, eliminating any residual medium. This design prevents cross-contamination between batches and helps clients successfully pass stringent GMP validation audits.
What materials are used for wetted parts to ensure corrosion resistance during CIP/SIP cleaning cycles?
Valve bodies are manufactured from CF8, CF8M, or 316L stainless steel with electropolished surfaces (Ra≤0.4μm). Seals are available in PTFE or EPDM, providing excellent resistance to acids, alkalis, and high-temperature cleaning agents.
Can KINKO provide full validation documentation for pharmaceutical projects?
Yes. We provide a complete validation package including material certificates, surface roughness reports, FDA compliance declarations, and third-party test reports. All documentation is available in bilingual format for international regulatory submissions.
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