FDA’s “Off-Label Risk Reduction” Approach to Reprint Distribution is “Misguided,” Says Sidney Wolfe
In June, the FDA issued a THIRD draft guidance document regarding reprint distribution by pharmaceutic companies. This new guidance describes FDA’s recommendations for distributing...
FDA Targets Companies for Facebook ‘Likes.’ Is Twitter ‘Favorites’ Next?
FDA Targets Companies for Facebook 'Likes.' Is Twitter 'Favorites' Next?
Why I Will Be Attending Digital Pharma East
Rich Meyer initiated quite a controversy on his World of DTC Marketing blog when he posted a "guest" article by an anonymous "Senior Director...
#mHealthEthics: A Call for Pharma to Develop Mobile Health “Guiding Principles”
According to a "Client Alert" from Pillsbury Winthrop Shaw Pittman LLP, FDA’s new draft guidance that would exempt from premarket 510(k) review many low-risk...
The Intricacies of Rx Drug Advertising! Learn Rules & Regulations from a Master
Pharmaguy interviews Preeti Pinto, former Executive Director & Head of Promotional Regulatory Affairs at AstraZeneca. We talk about the Advertising and Promotions Course that Preeti will teach at the Temple University School of Pharmacy this fall. Delve into the regulatory intricacies of Rx Drugs advertising!
What Types of Health Info Do Mobile Users Seek and Is It Relevant to...
You don't hear much about it, but pharma advertises on mobile devices. An Astellas marketing campaign for its overactive bladder drug, Myrbetriq, for example,...
Do PDUFA Fees Encourage Approval of Dangerous Drugs and/or Undermine FDA’s Regulatory Oversight of...
A new study by researchers from Cambridge Health Alliance/Harvard Medical School, Boston Medical Center (BMC)/Boston University School of Medicine (BUSM), City University of New...
Patient Storytelling Marketing: Creativity vs. Truth in Pharma Advertising
These days, patient storytelling is all the rage. More often than not, however, patient stories told by
pharma marketers are not 'providing truth' in the sense that they are real patient stories.
Patient Activists Demand Higher Quality Mobile Health Apps: Pharma Must Listen, Respond, and Optimize!
Sooner or later Congress, perhaps urged on by patient advocates or some mhealth app adverse event, may investigate the mobile health app industry -- including the drug industry -- to see if further oversight, not just FDA regulations, is required. Before that happens and to ensure that mobile health apps developed by pharma are of the highest quality, the industry should differentiate itself from "wild west" developers by being pro-active in developing and abiding by a set of 'Guiding Principles for Mobile Health Apps.'
Pharma Marketing News Vol. 13, No. 7: August 2014
Welcome to Volume 13, Issue #7 (AUGUST 2014) of Pharma Marketing News.















