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
My Profile
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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Category Archives: FDA
Advisory Committee Schedule for 2008
Rather late this year, the FDA has posted the tentative dates for advisory committee meetings for 2008. Right now, except for meetings that have already been announced, these are primarily "save the date" reservations so that the many experts on … Continue reading
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Hiatus Interruptus – Advisory Committees Set Meeting Dates
Hi there. I know I was taking this week off for vacation, but it hasn’t worked out that way. After a quick trip to the family, a 14 hour return drive, instead of R&R, I’m working again. So here is … Continue reading
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