Are You Ready for FDA FSMA Preventive Controls Audit? - Webinar (Recorded)

Overview:

This course will examine new FDA authority, introduces examples of Preventative Controls, leading into minimal recommended preparation steps for handling the new FDA FSMA requirements, including managing Form #483, or the FDA Warning for non-compliances.

Why you should Attend:

FDA implemented the new Food Safety Modernization Act (FSMA), including the hazard analysis and risk-based preventive in 2016 to help industry manage potential hazards in producing safe food products. FSMA places primary responsibility on the owners and operators of food facilities to identify and control hazard risks, and intentionally grants facilities considerable flexibility in designing and implementing their food safety plans. In light of these new regulations, FDA introduced an enhanced audit approach to ensure food processors have adequately eliminated these potential risks in their food facilities. Hugh liability potential for food companies not compliant with new FSMA regulations, Zero Tolerance with new Swabathons often resulting in Recalls, Senior Leadership as well as facility teams need to be knowledgeable of law, new authority and requirements. A prudent investment to ensure organization avoids costly mistakes.

Areas Covered in the Session:

Topic Background: Key FSMA Audit takeaway points would include:

• New FSMA requirements overview
• Minimal requirement recommendations for FSMA
• Essentials to build your own playbook, the Food Safety Plan
• HARPC, what’s new from former HACCP approach
• Documentation needs that are vital
• New Legal Authority
• Stats on #483’s