Hi all -
Point of confusion in BRC v7 clause 5.4.4.
I have a single program/procedure that covers the handling of any and all 'claim-labeled' product - non-GMO, Halal, process verified (USDA AMS), No Antibiotics Ever (ANE), etc. Supporting documentation for each claim is maintained elsewhere. Am I required to conduct and document a traceability/mass balance exercise for EACH specific type of claim, or just at the frequencies as required to demonstrate the viablity of the overall traceability system? At a minimum of 2X per year per claim, I could be looking at +20 traceability exercises a year...
Please tell me you can save me from unnecessary redundancy!
KTD