Monday, 15 October 2018

Free webinar - Cleaning Validation Top Challenges: What you need to know. This two-part Webinar presents three of the top issues that companies face today. In the first part, Dr. Tim Sandle challenges us to evaluate our sampling plan for assessing microbiological levels of contamination and discusses how to reduce this type of risk in the process. In the second part, Ms. Endisch introduces the idea of automation and data integrity, as the cleaning validation process is largely manual in the majority of organizations, and how this can help to provide a more scientific and justifiable process. She answers the question ‘how to do more with the resources I have’ in relation to calculating MAC (maximum allowable carry-over) levels and evaluating the worst case product, see:

Posted by Dr. Tim Sandle, Pharmaceutical Microbiology

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