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Avecia > Biologics >Quality > Quality Control

Quality Control

Quality Control (QC) support cGMP manufacture in Avecia’s manufacturing facilities. Analytical methods requiring development are first transferred to assay development before transfer to QC. Established, verified analytical methods are transferred directly to QC.

Avecia can offer a wide range of analytical services including:

    • microbiology - bioburden, organism identification, air/water monitoring
    • chemical analysis and traditional wet chemistry techniques
    • separation science - a range of chromatographic and electrophoretic techniques such as GC, HPLC, gel electrophoresis
    • structural characterisation - N+C terminal analysis,
      MALDI-TOF mass spectrometry
    • genetic characterisation - DNA sequencing, PCR
    • spectroscopy - UV/Vis, fluorescence, IR, ICP
    • biochemical - ELISA, bioactivity assays
    • further specialist knowledge and services ( e.g., LC-MS,
      CE, MS-MS, XRF, SEM ) are provided by specialist,
      audited partners

 


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Avecia Biologics, Billingham, UK

The Avecia Difference - quality control

 

 

 

 

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