FDA taps PatientsLikeMe to test the waters of social media adverse event reporting

Jun 16, 2015, 00:00 by Michael Croft

mobihealthnews | PatientsLikeMe has announced a research partnership with the FDA: The agency will assess the platform's feasibility as a way to generate adverse event reports, which the FDA uses to regulate drugs after their release into the market.

June 16, 2015 | PatientsLikeMe has announced a research partnership with the FDA: The agency will assess the platform's feasibility as a way to generate adverse event reports, which the FDA uses to regulate drugs after their release into the market. mobihealthnews