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Our experienced design and development engineers are using state
of the art tools.
All in situ sterilisable fermenter systems are designed and
manufactured in accordance with guidelines of the current Good
Manufacturing Practice (cGMP) in regard of hygienic and aseptic design of
process equipment and piping. A recorded QC is routinely performed during
production and delivery. Suitable adaptations can be made on request.
Our products meet common international quality and product safety
standards including applicable IEC and CE directives. The pressure
vessels are normally designed according to the PED Code for pressure
vessels. Design according to other codes can be made on request.
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