Quick question about paperwork review for forms or data generated by techs. Every lab or company I have been involved with always has a spot for someone to check, review, or verify the information on the paper. Is this an FDA requirement, and if so which CFR?
They only thing I have seen in the SQF code is under 220.127.116.11 which states "The methods and responsibility for undertaking monitoring activity, verifying, maintaining and retaining records shall be documented and implemented"
We have a lot of forms in place with no spot for a signature or review and I want to know if this is a requirement.