The FDA and other regulatory agencies have stated that software validation can only be accomplished effectively if "risk-based". How can this be done in the "real world". Why should you Attend: Software has become pervasive in medical devices themselves, and in the controlling, running and monitoring of medical product processes, whether they be in the pharmaceutical, medical device, biologics or dietary supplements industries. A quick review...

This series provides a comprehensive overview of advanced lighting systems, for both interior and exterior applications. This series covers lighting sources, technology applications, controls, emerging technologies and future trends. This series also covers federal purchasing requirements and specific agency requirements and resources. By completing this Series, participants will learn to: Identify various lighting sources and their most effec...