This document summarizes a presentation about data management in a regulated environment. It introduces two speakers from Medtronic who discuss the challenges of making changes to applications that require FDA approval. These include needing to revalidate applications every time a change is made. The presentation then discusses why MongoDB may help, including its flexibility and performance, but that noSQL does not mean no schema. It also notes gaps that need to be addressed like enterprise acceptance of new approaches and integrating MongoDB with reporting tools and making it 21 CFR Part 11 compliant.