‘In 2016 users will trust health apps more than their doctors’. So predicted Forbes Magazine in 2015 in reference to Mobile Health (“mHealth”) apps, E-Healthwhich are becoming increasingly popular to monitor health and well-being. However, the rapid proliferation of these apps with no clear evidence on their quality and reliability has raised concerns about the ability of consumers to assess their usefulness, thus potentially limiting their effective uptake for the benefit of public health.
In February 2016, following the results of an earlier public consultation, the European Commission (the “Commission”), appointed a working group to develop voluntary mHealth assessment guidelines (“Guidelines”). The purpose of the Guidelines is to provide common quality criteria and assessment methodologies to assist both consumers and healthcare practitioners in:

  • Deciding which app to use
  • Assessing the quality of each app with regard to clinical effectiveness
  • Ensuring the apps are in line with international standards

It was intended that the Guidelines be issued in four iterations and a third draft is expected before the end of 2016, with the final report expected to be published in January 2017.
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Source: Lexology, William FryBrian McElligot