2017 Medical Device Software

Software is ubiquitous in the world of medical technology, and is the source of many problems and enforcement actions. For the regulatory, quality, and product development professionals who manage and oversee software inside of or connecting their products, it can be difficult to interact most productively with IT professionals. This interactive workshop is specifically designed to help non-software professionals better understand what to look for and beware of, what questions to ask and decisions to make, and how to monitor products and systems for potential issues.

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