Sins of omission: how the US FDA's social media Inaction puts patients and industry at risk

Bill Drummy

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Sins of omission: how the US FDA's social media Inaction puts patients and industry at risk

机译：遗漏罪恶：美国FDA的社交媒体不作为如何使患者和行业处于危险之中

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Eighteen months ago, 80 of my closest friends and I presented before the US Food and Drug Administration on how the agency should regulate the promotion of medical products via the internet and social media. Not long after the November 2009 hearings, I wrote in this very publication: When might the agency issue some guidance for the industry? The smart money seems to be on "in about a year", and given that the opportunity for public comment extends until mid-February 2010, that seems like a reasonable bet.

机译：18个月前，我和我的80个最亲密的朋友向美国食品和药物管理局（FDA）介绍了该机构应如何通过互联网和社交媒体规范医疗产品的促销。在2009年11月的听证会后不久，我在这本出版物中写道：该机构何时可以为行业发布一些指导？明智的选择似乎是在“大约一年内”，考虑到公众发表评论的机会将一直持续到2010年2月中，这似乎是一个合理的选择。

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《Regulatory Affairs Journal- Devices》 |2011年第mayajuna期|共1页
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Bill Drummy;
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机译：遗忘的罪过：美国FDA的社交媒体不作为如何使患者和行业面临风险
2. FDA Gets Social Media Advice From Industry [J] . Owen Skoler Washington Drug Letter . 2010,第7期

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Sins of omission: how the US FDA's social media Inaction puts patients and industry at risk

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