On December 30, the U.S. Food and Drug Administration issued draft guidance focusing on how pharmaceutical companies should respond to unsolicited requests for off-label information about prescription drugs and medical devices. As of January 4, 2011, FDA is requesting public comment on the draft guidance document.
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Part of a Special Series on unNiched(micro) Scratch, Sniff and Learn Innovations
Part of a Special Series on Advanced Marketing and Measurement Techniques
Understanding How to Reach Customers Online, on Television, by Mail, E-mail and Other Media
Read more »In February 2011, AstraZeneca released a white paper focusing on the Food and Drug Administration's regulation of digital and social media. The paper also focuses on how pharmaceutical companies like AstraZeneca can operate in the digital realm before and after FDA releases guidance on how drug firms should market their products online.
In addition, the paper provides and overview of AstraZeneca's opinion on how FDA should regulate social media communications:
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