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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Category Archives: Podcast
FDA’s Dr. Janet Woodcock Discusses Adaptive Clinical Trials
We are all trying to re-enter the workforce after August. Here in the Beltway, the Congress is headed back and the traffic congestion returns as students everywhere return to school. Labor Day Weekend has passed and alas, I have put … Continue reading
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HIV in Africa – A Conversation with Former HHS Secretary Louis Sullivan
Last week the Bush Administration announced that it would be seeking a doubling of the U.S. commitment to fund HIV/AIDS care. That evening, ABC World News Tonight ran a story on the request and compared before and after photographs of … Continue reading
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FDA and Pharma Images – A Conversation with Patrick Clinton – Pharmaceutical Executive Magazine
As noted in this space many times, the images of the Food and Drug Administration as well as the pharmaceutical industry have been suffering greatly, most certainly in the post-COX-2 era. The result has been a rash of lawsuits, congressional … Continue reading
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Supplements and Adverse Event Reporting – A Conversation with the Council for Responsible Nutrition
As reported in the past here, the 109th Congress passed S.3546 – The Dietary and Supplement Non-Prescription Drug Consumer Act – legislation that would make it mandatory for manufacturers of dietary supplements and OTC products to report serious adverse events. … Continue reading
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Approvable Letters – A Conversation with Myself…
I am posting a podcast which, unlike past efforts, is not an interview, but a short discussion on my take on approvable letters. What makes an approvable letter more likely than an approval letter for investigational products? While there is … Continue reading
Posted in Approvable Letters, Podcast
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