Webinar: Critical Process Cleaning & Cleaning Validation

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

Speakers:

frank kohn Profile Pic

Frank Kohn
President, FSK Associates, Inc

LinkedIn: https://www.linkedin.com/in/frank-kohn-593b8712

 

 

Susan Cleary
Director Product Development, Novatek International

LinkedIn: https://ca.linkedin.com/in/susan-cleary-15485b3

Register Below to Access the Recording!

Simply provide your information below and Novatek will e-mail you the access information to watch this webinar recording any time convenient to you!

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!

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