Hello,
I am looking for feedback on a supplier questionnaire I’ve just drafted up. In particular, I have some uncertainty about section 4.1. I don’t intend to come across as if my company views all of these supporting documents as necessary, but that we would appreciate them on file if available. I’ve formulated the current list of documents based on what we’ve been asked for in questionnaires that we’ve received.
For some context, I am the entirety of the quality dept. of a small business in Canada that operates in primarily probiotic+prebiotic products sold business to business to animal food and supplement companies. We are not currently GFSI certified, but I am working on improving our supplier and raw material risk assessment and approval processes, which has lead me to developing this supplier questionnaire.
I’m trying to hit a balance between being useful and giving use information that actually impacts our supplier risk assessment, while not being a 20+ page questionnaire that is a pain to fill out. That, and some posts I’ve seen on these forums, is what led me to directing GFSI-certified suppliers to skip what is effectively redundant questioning.
Any feedback at all is much appreciated!