About the Author
My name is Mark Senak. I’m a lawyer and I work at the international communications firm FleishmanHillard in New York. For the past several years, I have been consulting with pharmaceutical and biologic companies that are engaged in the process of bringing new drugs to market. I have also worked extensively with an array of medical societies and patient organizations providing strategic communications counsel and media training.
Daily Archives: March 20, 2008
Better Late than Never? FDA Oks Slower Approvals
As mentioned in yesterday’s post, the FDA has signaled that due to work burden, the agency will be allowing PDUFA dates to be missed… The RPM Report got the lowdown from John Jenkins, director of the Office of New Drugs … Continue reading
Posted in FDA Policy
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