Validation of sterilizing filtration
20 April 2018
• To understand the key control measures and they impact the sterility assurance of the product
• To introduce new thinking for qualification & validation based on risk assessment
• To follow the EU GMP and cGMP regulations and guidelines for aseptic processing and to engage in discussions regarding industry changes and best practices
Anyone who wants to know more about GMP, such as quality control, quality assurance, and operations staff who perform GMP activities.
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