About the AuthorMy 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.
My ProfileI 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 BlogEye on FDA is published by Mark Senak of FleishmanHillard's Washington, D.C. 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: May 4, 2009
Tomorrow at noon my employer will be holding a Webinar with the above title featuring myself, Jeff Levi of Trust for America's Health, and my colleague Christina Pearson, former Deputy HHS Secretary for Public Affairs. How To Register System … Continue reading
Eight years ago, the FDA was a gold standard agency. Today that gold is tarnished by eight years lacking in leadership, vision and growth with the times. High level mis-steps and a lack of momentum has caused a crisis in … Continue reading