Medical Device SOP Advisors maintains a database of customers and their purchased SOP’s. When we update a standard operating procedure because of FDA or ISO mandated changes we will notify you. Updated SOP’s will be available for sale at half the cost of the original. You can be assured that your medical device Quality Assurance System and Quality Manual will always meet FDA GMP / QSR requirements and not expose you to possible FDA 483 compliance observations for your medical device documentation.
Click on "SOP's Available" to see descriptions of the SOP's available for sale