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GE Healthcare Institute9/3/2014
Santa Clara, CA9/10/2014
10/1/2014 - 11/30/2014
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Welcome to Regulatory Reconnaissance, your daily regulatory news and intelligence briefing.
Brazil's medical device industry should prepare for electronic submissions, Anvisa, Brazil's national regulatory agency, said at a 20 August 2014 meeting.
Earlier this year, the US Food and Drug Administration (FDA) released a much-anticipated draft guidance document which could potentially expand the ways in which pharmaceutical and medical device companies could distribute information regarding the safety of their products, even if that information isn't for an FDA-approved indication.