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Detailed overview of FDA FSMA rule, leading into recommended preparation steps for handling the new FDA FSMA audit when investigators come to your door. Drilling down, will focus on Food Safety Plan hazards or Hazard Analysis Risk Preventative Controls (HARPC), the importance of the Preventative Control Quality Individual (PCQI), with documentation requirements. The Webinar will also cover how to handle a "Swabathon", where FDA's new RTE (Ready To Eat) Listeria Monocytogenes Guidance may come into play, and expectations for FDA FSMA audits
Why should you attend this webinar?
FDA expectations on the new Preventative Controls audits are daunting, if one is not prepared it could result in non-compliances or #483, or worse for an organization. This webinar will detail the watch-outs and best approaches to manage FSMA
Areas Covered in the Session:
Who can Benefit:
Speaker Profile :
Gina Reo, is a Keynote Speaker at Compliance Key. She is the President, QAS, (Quality Assurance Strategies, LLC), private consultation for the Food and Beverage Industry specializing in Global Food Safety and Quality with expertise in Regulatory Compliance, Prop 65, Crisis Management, Business Integration, and Due Diligence M & A Compliance Risk Assessments.