Will your food fraud vulnerability assessment pass an audit?

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Will your food fraud vulnerability assessment pass an audit?

Will your food fraud vulnerability assessment pass an audit?

When and where

Date and time

Location

Online

Refund Policy

About this event

Date: Nov 11, 2022

Time: 1 PM EST

Duration: 60 Minutes

Level: Intermediate to Advanced

Group Packages: Please contact ben@complyrules.com

Description

The webinar will provide you with valuable information about setting up a food fraud vulnerability assessment so that you are better prepared to meet the food fraud-related requirements of GFSI Certification Programme Owners and the economically motivated adulteration requirements of the U.S. Food Safety Modernization Act.

Why Should You Attend:

GFSI and Certification Programme Owners require that documented food fraud vulnerability assessments and control plans be put in place in order to meet audit requirements. The U.S. FDA has also implemented additional requirements related to prevention of economically motivated adulteration. Do you have a good understanding of how to put this in place and where you can source the information to support your assessment? This webinar will address these new requirements and walk you step by step through the tools and resources available to support you in meeting food fraud mitigation audit requirements.

This webinar will present historical background on food fraud with presentations of specific incidents and lessons learned. The presenter will also discuss details of new U.S. FDA Food Safety Modernization Act and Global Food Safety Initiative requirements related to prevention of food fraud and economically motivated adulteration. The presenter will give an overview of various tools available to support the conduct of vulnerability assessments by the food industry, with a brief description of some of the similarities and differences within each. Finally, a discussion of what is currently known about how auditors are approaching an assessment of food fraud requirements will be presented.

Areas Covered in the Webinar:

  • Historical background on food fraud
  • Presentations of specific incidents and lessons learned
  • Details of new U.S. FDA Food Safety Modernization Act requirements
  • Details of new Global Food Safety Initiative requirements
  • Overview of various tools available to support the conduct of vulnerability assessments
  • Brief description of some of the similarities and differences within each tool
  • A discussion of what is currently known about how auditors are approaching an assessment of food fraud requirements
  • Discussion of Decernis and related tools

Who Will Benefit:

Food safety specialists, food safety and defense coordinators, quality scientist, head of quality assurance, etc. from the food industry

Important: Please plan to bring a multidisciplinary group from your Company to gain the most from this very important seminar.

  • In-Person Seminar going Virtual with increased learner satisfaction.
  • Yes, attend this seminar from anywhere. We are making it real and more interactive – Here's a sneak peek:
  • Our enhanced delivery process and technology provides you with an immersive experience and will allow you to access:
  • The real-time and live presentation as in in-person events
  • Private chat for company-specific conversation – the same as you would get in an in-person seminar
  • Opportunities to connect with your peers to share knowledge at different times and have group discussions
  • Live workshop activities
  • Live Q&A during the event and offline Q&A assistance after the event
  • As usual more content, activities and case studies and now adding homework for a comprehensive understanding

Additional service: (Personalized session)

We also do various similar customized events for our clients and it is specially tailored as per the client's requirement. We arrange calls between clients and our course instructors to better understand the training requirement and accordingly a training program is designed. The course duration ranges between 90 Mins and 12 hours. Most 6 hours and 12 hours of classes are split into 2 to 3 days considering customer convenience.

We have 500+ consultants who are associated with us and each have their own specialization example GxP, GMP,GLP, 21 CFR, Computer system validation, FDA Audit & Inspection, Bioassays, Design Control, Data Integrity, FDA regulation, Clinical compliance, and almost everything that falls under Risk, Quality and Compliance arena in the Life Science industry.

If you think that your team needs some kind of boost, update or refresher in Risk management and Regulatory compliance then let me know and we can design a highly cost efficient program for you.