Best Practices in Preparation for an FDA Computer System Audit - March 10, 2021 - CA US
March 10, 2021 - CA US Compliance4All Phone:8004479407 Overview: As a "GxP" system, following Good Manufacturing, Laboratory and Clinical Practices, the computer system must be validated in accordance with FDA requirements. If electronic records and/or electronic signatures (ER/ES) are incorporated into the system, FDAs CFR Part 11 guidance on ER/ES must be followed. This webinar will focus on the key areas that are most important, including security and dat...
System Development Life Cycle Best Practices System Auditmarch Good Manufacturing Clinical Practices அமைப்பு வளர்ச்சி வாழ்க்கை மிதிவண்டி
Source: lifescienceleader.com