V5 talked about a supplier approval procedure; V6 now asks for a documented risk assessment on each raw material.
If a product questionnaire that is filled out by the supplier asks questions about allergen, foreign body, mirco and chemical contamination risks, does its review when it is returned constitue a "risk assessment". Can the questionnaire be stamped and signed off as Approved (or otherwise if not satisfactory) or does all the information have to be lifted out and processed separately?
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