Center for Professional Innovation & Education, Inc., Los Angeles, CA
June 13 & 14, 2013
This course provides practical guidance on cleaning validation regulatory compliance, in conjunction with, risk-based, reasonable and informed decision making and activity planning. The program will describe the requirements for establishing an effective cleaning validation program, including the development of a general policy, a “Cleaning Validation Master Plan” and the appropriate documentation for each study to be performed. In addition, requirements for maintenance of the validated status will be reviewed. Regulatory requirements and the latest industry practices will also be included in the discussion. Cleaning validation examples from pharmaceutical, biologic and biopharmaceutical manufacturing processes will be included.
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