You have a Sterility Failure or Bioburden Excursion - Now What? 2013 is a webinar that covers topics such as:
- 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?
You have a Sterility Failure or Bioburden Excursion - Now What? 2013 brings together:
- Validation specialists
- QA personnel
- R&D specialists
- Manufacturing personnel involved in validations