Are You Ready for new FDA FSMA Audit?

Instructor: Gina Reo
Product ID: 705949
Training Level: Basic to Advance
  • Duration: 60 Min
This FSMA audit webinar will explain the 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 for non-compliances.
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Read Frequently Asked Questions

Why Should You Attend:

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.

Important Learnings:

  • Expectations covered for new requirements for FSMA Audit by Regulators
  • New Hazard Analysis Risk Preventative Controls (HARPC) or Food Safety Plan basics introduced
  • Employee preparation and training essentials explained
  • Supply chain Preventative Controls outlined
  • Legal Authority of FDA detailed, including watch-outs
  • Importance of documentation requirements described
  • Closing a Successful Audit, including managing #483’s and confidentiality

Areas Covered in the Webinar:

  • New FSMA requirements overview
  • Minimal requirement recommendations for FSMA
  • Key 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
  • Preventative Controls
  • Supply chain Preventative Controls
  • Insights & Success Takeaways

Free Materials:

  • References cited
  • Rule documents or guidance
  • Form examples

Who Will Benefit:

  • Quality Control/Assurance and Food Safety professionals
  • supervisors, leads, managers
  • Operations managers/supervisors
  • Sanitation managers, supervisors or leads
  • Corporate quality managers; Operations personnel
  • Senior management
  • PCQI’s
  • Plant management personnel
  • Third parties developing HACCP plans
  • Auditors and those with food safety inspection roles
  • Validation specialists
  • Consultants
  • Quality system auditors
Instructor Profile:
Gina Reo

Gina Reo
President, Quality Assurance Strategies LLC

Gina Reo, 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.

Formerly, Vice President, Food Safety, Weston Foods (WF), a GWL Canadian company and North American leader in bakery products. Transformed organization toward World Class Excellence for Food Safety within four years by framing Food Safety Roadmap Strategy for fast-tracking compliance to FSMA (Food Safety Modernization Act), SFCA (Safe Foods for Canadian Act) and new NLEA (Nutrition Labeling Education Act) for US and Canada compliance.

Over 25+ years of food safety and quality experience, after holding successive senior positions with Colgate-Palmolive, Coca-Cola, Bestfoods NA, Unilever, YUM! Brands and Quiznos (Board). Prior to joining Weston Foods, held position of Quality Director with Mondelez International (formerly Kraft Foods) in Europe, (Zurich, Switzerland) and Cadbury as QA Chocolate Director (Quality, Environmental, and Health & Safety) for NA/Europe/Global.

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Human Error Reduction Program

Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

If you have any concern about the content of the webinar and not satisfied please contact us at below email or by call mentioning your feedback for resolution of the matter.

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