DUBLIN--(BUSINESS WIRE)--The "FDA Modernization and Restructuring of the SDLC for Computer System Validation and Compliance" webinar has been added to ResearchAndMarkets.com's offering. You will learn ...

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 ...

The attendee will learn about how to take advantage of modern, evolving technology while remaining compliant with FDA regulations related to computer systems and data. We will discuss ways to ...