APR 14, 2016 7:00 AM PDT

WEBINAR: Avoiding the Pitfalls When Automating Cell Viability Counting for Biopharmaceutical Quality Control

  • Senior Marketing Manager, Beckman Coulter
      Tony held the Convenorship of the ISO Working Group revising ISO 14698-1 & -2 for microbial control in cleanrooms and was the UK subject matter expert to the ISO Working Group who issued the 2015 revised versions of the ISO 14644-1 & -2 documents for cleanroom classification at the heart of the aseptic manufacturing chapters of both the European GMP and the USA cGMP documents. Tony was joint editor on the ISPE Guide to Ozone Sanitization of Pharmaceutical Water Systems and was also chief editor of the PHSS Best Practice Guide for Cleanroom Monitoring. Tony is employed by Beckman Coulter Life Sciences as a Senior Manager.

    April 14, 2016, 7:00am PT, 10:00am ET, 2:00pm GMT

    Whether cells are being used to manufacture a therapeutic drug product or for pharmacology, measuring the cell viability and concentration accurately and with good reproducibility is crucial. This presentation describes how to avoid the common pitfalls when adopting a new, automated method of cell counting.

    Learning Objectives:
    • Learn key critical elements of automated cell viability counter adjustment for correct cell counting
    • Learn key pitfalls when automating cell viability counting

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