Wednesday November 9th, 2016 1:30PM – 2:30PM EST
Stay in touch with the best practices in Cleaning Validation. This webinar will outline a Risk-Based Life cycle approach to Cleaning Validation. We will discuss Risk Management components for design and development of Cleaning Validation Programs and approaches.
Topics covered include:
- Review of the cGMP issues in Cleaning Validation
- Several examples of FDA 483 items and other regulatory bodies will be discussed
- Different approaches to answering the question on “How do I establish acceptance criteria?”
- Real case study will be used as an example on how to perform a Risk Analysis
- Data management and sampling for cleaning validation will be presented
President, FSK Associates, Inc
Director Product Development, Novatek International
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Stay up to date as Novatek will be offering many more educational webinars in 2017. Thanks for your interest we look forward to your attendance in the future!