I need help, please! Our company is FDA and SF/SF regulated. Our quality management document system used to be paper-based with PDF copies on an internal server to allow employees access to procedures and forms. We are now working on moving all documents to another server with a website-type set-up. It will be a repository for the Quality Management System. It will not contain any constantly updated "live" docs. We have to validate it, but since it's "home-made" so to speak, we're not sure how to accomplish this.
Does anyone have a similar validation that we could view and follow as a template?
Thanks for taking the time