You have a Sterility Failure or Bioburden Excursion - Now What? 2013
07 Mar 2013
Webinar
Key Topics
What items are important to investigate during sterilization process validation?
Is this result really a failure that needs to be investigated?
The lab says the routine process BI is positive, what now?
If a failure occurs during sterilization process validation what actions can you take?
The periodic bioburden testing exceeded the established alert limit, what actions should be taken?
My dose audit did not pass, what does that mean?
How to determine if the bioburden excursion has an impact to sterilization
What do you do if the bioburden action limit is exceeded?
Who should Attend
Validation specialists
QA personnel
R&D specialists
Manufacturing personnel involved in validations
Past Events
You have a Sterility Failure or Bioburden Excursion - Now What? 2013 - 07 Mar 2013, Webinar (14817)
You have a Sterility Failure or Bioburden Excursion - Now What? 2026
Important
Please, check "You have a Sterility Failure or Bioburden Excursion - Now What?" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Medical device, Medical laboratories, Pharma
