FDA FSMA Preventive Controls Inspection Hot Buttons for 2022

Speaker

Instructor: Gina Reo
Product ID: 705949
Training Level: Basic to Intermediate

Location
  • Duration: 60 Min
This course will look at the new FDA direction and other programs aimed at transforming food safety in 2022 and beyond, including how to manage #483 violations for non-compliances.
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Why Should You 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. Along the way, implementation has taken a few twists and turns, including side-tracking with a pandemic.

So, what have we learned along the way and where is the FDA now focused with Food Safety improvements? 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. However, not all the industry has stepped up to mitigate risks effectively.

Key FSMA takeaway points are covered, with requirements overview explained with the minimal recommendations for successful FSMA compliance. Key Essentials to examine your own playbook, the Food Safety Plan (HARPC) are teased out in detail.

Documentation needs with an in-depth review of Preventative Controls the main focus of FSMA for food processors and mandatory Supply chain Preventative Controls are explained as well.

Also covered will be tools, legal implications and best practices for industry professionals.

Areas Covered in the Webinar:

  • Expectations covered for new 2022 FSMA Audit by Regulators
  • Hazard Analysis Risk Preventative Controls (HARPC) or Food Safety Plan basics covered from FDA identified gaps perspective
  • New World Post FSMA, understanding new regulations
  • COVID, a Bump in the Road or a New Normal
  • Robust Food Safety Plan, Know Your Site and Programs, what you need for your own Food Safety Plan
  • Required Documentation
  • Sanitation Program to mitigate risks and watch-outs
  • Environmental Monitoring Programs Essentials
  • Other Needed Risk Mitigation Programs
  • Employee Training Program Importance
  • Corrective and Preventative Action (CAPA)
  • Understanding Verification vs. Validation Programs
  • Supplier Programs, recommended minimization requirements
  • Next Steps

Who Will Benefit:

  • PCQI, Food Safety Teams, QA, Plant leadership, OPS, Regulatory, R & D, Sanitation Teams, supervisors, front line leaders, maintenance leaders, technicians, 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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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. We respect feedback/opinions of our customers which enables us to improve our products and services. To contact us please email [email protected] call +1-888-717-2436 (Toll Free).

 

 

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