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WIKA – Measurement technology for the pharmaceutical industry

Wika Instrumentation Corporation is a trusted partner of T.V.P. Co., Ltd. with T.V.P. distributing a wide range of its measurement products.

In view of higher demands on quality and product safety from pharmaceutical production, sterile process engineering plays a significant part in the cost-effectiveness and safety of production processes, in both upstream and downstream areas. Even in the further course of the process chain, contamination-free processing is a crucial quality factor. This demands a combination of the most up-to-date hygienic design and, at the same time, a high measuring accuracy.

GMP compliant

Measuring instruments from WIKA are manufactured in line with the GMP guidelines (good manufacturing practice). They meet the stringent requirements of:

  • FDA (Food and Drug Administration)
  • EHEDG (European Hygienic Engineering & Design Group)
  • 3-A Sanitary Standards, Inc.
  • ASME BPE (Bio Processing Equipment)
  • ATEX (directive 94/9/EC)

For the proof of conformity within the scope of an FDA approval and national authorities, we have an extensive program ready-certified. For the ongoing testing of the instruments in the context of quality management, a wide range of calibration equipment and calibration services are available.

Process connections

WIKA supplies a wide range of industry-standard and manufacturer-specific process connections in hygienic design, for example:

  • Clamp connections, Tri-clamp, DIN 32676, ISO 2852, ASME BPE (most common in Thailand)
  • Aseptic connections DIN 11864
  • NEUMO BioConnect® and NEUMO BioControl®

For toxic, bioactive substances or very sensitive substances, special instrumentation options are available in order to integrate the measuring instruments into the plant without elastomers.