What to Expect with the new FSMA Intentional Adulteration Regulation

The session will explain coverage and will summarize requirements for facilities that manufacture, process, pack or hold human food. It will also discuss exemptions, as well as best practice approaches and Food Defense Qualified Individual in detail.

Gina Reo
Instructor:
Gina Reo
Date:
Friday, April 24, 2020
Time:
10:00 AM PDT | 01:00 PM EDT
Duration:
60 Minutes

More Trainings by this Expert   Product Id : 502962

Price Details
$150 Live
$290 Corporate Live
$190 Recorded
$390 Corporate Recorded
Combo Offers
Live + Recorded
$289 $340 Live + Recorded
Corporate (Live + Recorded)
$599 $680 Corporate
(Live + Recorded)
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Overview:

IA establishes requirements to prevent or significantly minimize acts intended to cause wide-scale public health harm.

The session will explain coverage, summarize requirements for facilities that manufacture, process, pack or hold human food. Also, exemptions will be discussed as well as best practice approaches and Food Defense Qualified Individual detail.

Why should you Attend: FDA 's new Intentional Adulteration Regulation launched in July, 2019 is a significance addition to the list of FSMA (Food Safety Modernization Act) requirements and the last of its foundational rules.

The intent is to seamlessly augment existing systems for food manufacturers, however there are new requirements that must be incorporated.

Compliance dates, requirements, Key Activity Types (KAT), Hybrid Approaches, defining, de-risking and preventing an attacker, mitigation strategies, Fundamental Elements, creating a Food Defense Plan, point, step, or procedure (PSP), actionable process steps (APSs), Vulnerability Assessment, recordkeeping, Training, Food Defense Plan Builder, and other important details will be outlined.

Areas Covered in the Session:

  • Food defense plan
  • Vulnerability assessment (VA)
  • Mitigation strategies
  • Procedures for food defense monitoring
  • Food defense corrective action procedures
  • Food defense verification procedures
  • Reanalysis
  • FDA Rollout Plan
  • Training
  • Records
  • Takeaways

Who Will Benefit:
  • Quality and Food Safety staff/mgt
  • PCQI Members
  • Operations Leads/Supervisors
  • Sanitation Leads/Supervisors
  • Plant Management
  • Warehousing Managers/Leads
  • Maintenance and Engineering Leads/Supervisors
  • Procurement Team Leads
  • Crisis Coordinators
  • Company Leadership
  • Risk Managers


Speaker Profile
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 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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