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.Stay Connected
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I am an authority on regulatory aspects of communications and medical products, with particular emphasis on pre-approval communications; strategist to help pharma and biotech companies prepare best case for advisory committee approval; and counselor in issues and crisis management. I am a frequent speaker on various aspects of same - drug development, promotion, reimbursement and new media in a highly regulated environment. Author of books, newspaper and magazine pieces related to drug marketing and promotion as well as HIV specialty pieces. And of course... blogger!About This Blog
Eye on FDA is published by Mark Senak of FleishmanHillard’s New York office. The thoughts and ideas in this blog and postings are strictly my own and are not screened by my employer. Everything posted on this blog is my personal opinion and does not necessarily represent the views of FleishmanHillard or its clients.
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Daily Archives: September 18, 2009
FDA to Hold Part 15 Hearing on Social Media and Pharma – Finally!
This is nothing less than astounding. The FDA is seeking input on social media and pharma. The hearing will be held on November 12 and 13 in Washington DC. Details are here. I have often railed against the DDMAC … Continue reading
Posted in FDA Policy, New and Social Media
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Weekly Roundup – 9-18-09
Well, now that the summer is over and Congress is back from their "recess" I decided it was time to bring back the Weekly Roundup as there is more happening in DC than usual and I'm more back in the … Continue reading
Posted in Weekly Roundup
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