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Food, Pharmaceutical & Biotechnology Applications

Supplier: Outotec
13 March, 2009

As this is such a diverse category all of the Larox products find application in this area. To determine the best equipment for your process please contact your closest Larox Sales Manager or Agent or click on the links below for more information:

Larox has the ability to build and deliver cGMP compliant solid-liquid separation equipment. In those cases we can also provide several levels of qualification documentation and testing as indicated below:

Qualification documentation and testing

  • Larox has entered into co-operation with Elomatic Oy to provide a wide range of commissioning and qualification services to Pharmaceutical and Biotech industries
  • We can provide different documentation and service packages depending on the customer demands
  • Standard Documentation Package (SDP) includes all the necessary documents and testing for the reliable operation of the filters
  • Compliance Documentation Package (CDP) includes all the documents necessary for the qualification of the filters according to the cGMP. This package includes also FAT and SAT protocols and testing
  • Qualification Documentation Package (QDP) includes documented risk analysis of the filters operation as well as IQ and OQ protocols
  • Extended Documentation Package (EDP) can include customer defined documents and testing that are not covered in the other documentation packages