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Differences between BRC 5.4 - Authenticity and IFS 4.3 - Product Fraud

Started by , Jan 08 2023 06:34 PM
1 Reply

OUR FACTORY HAS BOTH THE BRC AND IFS SYSTEM, OR DO WE HAVE TO ASSESS FOR EACH STANDARD SEPARATELY

BECAUSE I THINK THAT WE HAVE MADE AN IFS COUNTERFEIT RISK ASSESSMENT AND A LIMITATION PLAN, IT COUNTS WITH AUTHENTICITY
DOES HE UNDERSTAND WRONG?
 
ADDITIONALLY I HAVE A QUESTION
IN SECTION BRC 3.5 WHEN ASSESSING A RAW MATERIAL RISK, THE ISSUE OF REPLACEMENT AND FRAUD SHOULD BE TAKEN INTO ACCOUNT.
COULD IT NOT BE TAKEN INTO ACCOUNT IN THIS ASSESSMENT ONLY SEPARATELY AS A PRODUCT FRAUD?

 

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Differences between FSMA, VQIP and FDA Audits PRPs , GMPs , GHP , GSP , GAP , what is the differences ? Differences between non conformity and incident in FSMS What are the differences between a Risk Assessment Matrix and a CCP Decision Tree? Differences Between Withdraw and Recall
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OUR FACTORY HAS BOTH THE BRC AND IFS SYSTEM, OR DO WE HAVE TO ASSESS FOR EACH STANDARD SEPARATELY

I think YES because BRC/IFS text responses are often probably too different/difficult to combine unless you can produce a (combined) Manual(s) which an Auditor can readily understand. (Although examples of some combined manuals do exist on this Forum, eg ISO9001/BRC). Some people here are certified to multiple GFSI Standards so should have some input on yr query.

 

BECAUSE I THINK THAT WE HAVE MADE AN IFS COUNTERFEIT RISK ASSESSMENT AND A LIMITATION PLAN, IT COUNTS WITH AUTHENTICITY
DOES HE UNDERSTAND WRONG?
Sorry, I am not familiar with IFS.
 
ADDITIONALLY I HAVE A QUESTION
IN SECTION BRC 3.5 WHEN ASSESSING A RAW MATERIAL RISK, THE ISSUE OF REPLACEMENT AND FRAUD SHOULD BE TAKEN INTO ACCOUNT.
COULD IT NOT BE TAKEN INTO ACCOUNT IN THIS ASSESSMENT ONLY SEPARATELY AS A PRODUCT FRAUD?
If you are referring to Fraud in 3.5.1.1 and Fraud in 5.4.2, you can answer the Fraud requirements  in either Clause and use a cross-reference.

 

(Also see related thread -

https://www.ifsqn.co...nt/#entry192297

 


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