Demonstrating Equivalency and Limit of Detection for a Rapid Sterility Method via ATP-Bioluminescence
Now, more than ever, the pharmaceutical industry needs a rapid sterility test method. However, the validation of an alternative rapid technology proves too challenging for many QC micro labs. This reality is changing through the ongoing collaboration and sharing of validation strategies.
Utilizing an amplified ATP bioluminescence detection method, this presentation will share how equivalency, specificity and limit of detection was demonstrated against the compendial sterility method for membrane filtration, bringing the 14-day incubation test down to 6-days.
Presentation Date and Time:
July 28th, 2020 @ 11:00 am (central time zone)
Brice Chasey, Sr. Product Manager, Charles River Labs
|Introduction||11:00am – 11:05am*|
|Presentation||11:05am – 11:50am*|
|*Central time zone|
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