FDA's New Import Program Concerning International Consequences | 2 Day Seminar | Minneapolis, MN
August 31st & September 1st 2015| 2 Day - Minneapolis, MN
With what you learn in this seminar, you can work more productively and mitigate the risk of FDA detention. A high-ranking ex-FDA insider will give you straight talk on how FDA operates and the agency’s mindset. You will learn practical information, such as how to interact with FDA, the options you have to resolve problems and how you can prevent problems in the first place.
Speaker: Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. His comments are candid, straightforward and of practical value.
He understands how FDA thinks, how it operates and where it is headed. Based on his exceptionally broad experience and knowledge, he can synthesize FDA’s domestic and international operational programs, institutional policy and thicket of legal variables into a coherent picture.
For more details contact Complystream call us at: (+1) 844 498 6361
FDA's New Import Program Concerning International Consequences | 2 Day Seminar | Minneapolis, MN
August 31st & September 1st 2015| 2 Day - Minneapolis, MN
With what you learn in this seminar, you can work more productively and mitigate the risk of FDA detention. A high-ranking ex-FDA insider will give you straight talk on how FDA operates and the agency’s mindset. You will learn practical information, such as how to interact with FDA, the options you have to resolve problems and how you can prevent problems in the first place.
Speaker: Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requirements. His comments are candid, straightforward and of practical value.
He understands how FDA thinks, how it operates and where it is headed. Based on his exceptionally broad experience and knowledge, he can synthesize FDA’s domestic and international operational programs, institutional policy and thicket of legal variables into a coherent picture.
For more details contact Complystream call us at: (+1) 844 498 6361
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