LuminLogic, developed by MethodSense, Inc., is a 21 CFR Part 11 compliant med device management suite (SaaS) solution that supports document, regulatory, quality, and risk management systems for medical device, pharmaceutical and biotech companies during the commercialization process. Improve communication and teamwork across departments and functional areas with integrated collaboration and workflow tools. LuminLogic’s med device management suite makes it easy to globally access, create, modify, approve and electronically sign documents.
With LuminLogic Medical Device QMS Software there is an array of features and customizable solutions, you’ll be able to create quality and regulatory systems that meet your business’ evolving needs. Create custom configured applications quickly, and share them with your co-workers in real time. Our intuitive wizard guides you in building and maintaining custom applications yourself… no coding required! Connect with one of our regulatory software experts to get a live demo of Methodsense’s LuminLogic in action. We’ll show you how easy it is to use, as well as how it works to support the regulated environment your business supports.
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