WHITEPAPER: mHealth Regulations: Global Efforts and Readiness

July 20, 2015
Mobile health (mHealth) has become a disruptive force in healthcare, changing the way clinicians and patients interact with technology. With the development of a wide range of mobile applications within healthcare, regulatory agencies must rethink the very definitions of medical devices. While patient safety and privacy are paramount, many stakeholders are advocating for regulations that do not stifle innovation. Regulatory agencies and legislators, in response to active advocacy by the industry and end users, are shaping policy to ensure innovation is not hampered by the need for patient safety. The pressure on governments to devise better and more balanced legislation on mHealth is constant. Download this white paper. Discover how establishing a pro-innovation regulatory environment is critical to fueling innovation in mHealth to address the top priorities of value-based care.

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