Article | May 16, 2014

FSMA Fridays: What Constitutes A Good FDA Audit? (Part Three Of Four)

Source: Safety Chain Software

Part 1 | Part 2 | Part 3 | Part 4

On the last Friday of every month, Barbara Levin of SafetyChain, a leading provider of food safety and quality assurance automation and compliance solutions, hosts FSMA Fridays™, the leading online forum for the food and beverage community to learn the latest information about the FDA’s Food Safety Modernization Act (FSMA). Featuring Dr. David Acheson, the popular monthly interactive pod/webcast is sponsored by SafetyChain Software and The Acheson Group.

In the second portion of FSMA Fridays: What Constitutes A Good FDA Audit? Barbara Levin and the Acheson Group Panel discussed the key elements of a successful FSMA audit, and what good manufacturing practices (GMP) are necessary to be reviewed in an FDA audit. Additionally, the group will discuss the quantity and quality of the auditors needed for FSMA audits, along with the implications of not having enough qualified auditors. Here, in part three, the panel takes questions from the pod/webcast’s live audience.

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