I am having the hardest time trying to figure out how to validate documents etc. We are SQF certified and currently I have file cabinets full of paperwork and doing it the old school way and the auditor hasnt marked us down for it. We are switching to a new format and trying to go digital this next year. Currently we (managers) signoff on the daily documents as a way to verify that the work has been done and that documents have been reviewed. How is everyone doing this on digital software programs? Right now Im having to pull up the document digitally sign it and resave it. This is taking so much time (more than just signing the paperwork and filing it). The way I have understood the FDA is that we have to show (sign off) on documents within 7 days of completion and this is the standard we have been holding to with the paper documents. I pull monthly and quarterly reports and analyze the data and report on that for different production or sanitation documents. Are we over doing it? Also, are there any documents that we should not be doing digitally? I would like to move all production, sanitation, maintenance forms etc to a digital platform and store them in the cloud instead of my filing cabinet
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