WHO WE ARE

We specialise in systems for Clean in Place (CIP) and Sterilisation in Place (SIP) of process equipment in the pharmaceutical and biotech industries. We also provides consultancy within qualification and validation. Established 2007 with offices and test facilities in Denmark.

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PROCESS CLEANING

  • CIP / SIP systems
  • Test Facilities
  • Maintenance
  • Courses in Process Cleaning
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VALIDATION SERVICE

  • Installation Qualification (IQ)
  • Operational Qualification (OQ)
  • Performance Qualification (PQ)
  • Cleaning Validation
  • Courses in Quality from the suppliers perspective
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