In view of the high demands on the quality and product safety from pharmaceutical production, sterile process engineering plays a significant part in the cost-effectiveness and safety of the production processes, in both upstream and downstream areas. Even in the further course of the process chain, up to cleaning and sterilisation, contamination-free processing is a crucial quality factor. From measuring instruments, this demands a combination of the most up-to-date hygienic design and, at the same time, a high measurement accuracy.
re WIKA measuring instruments GMP-compliant?
Measuring instruments from WIKA are manufactured in line with the GMP guidelines (good manufacturing practice). They meet the stringent requirements of, e.g.:
For conformity verification with certification through the FDA and national authorities, we have a comprehensive programme of certificates available. For the ongoing testing of the measuring instruments in the context of quality management, a wide range of calibration equipment and calibration services are available. Which process connections are available for integration into pharmaceutical process plants?
WIKA supplies a wide range of industry-standard and manufacturer-specific process connections in hygienic design, for example:
Which instrumentation options are available to integrate measuring instruments into plants? For toxic, bioactive substances or very sensitive substances, special instrumentation options are available in order to integrate the measuring instruments into the plants without elastomers. |
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