Casper E. Uldriks

Casper E. Uldriks is the senior regulatory counsel in the Food and Drug Administration’s (FDA) Office of Compliance in the Center for Devices and Radiological Health. He manages the development of FDA’s postmarket guidance, policy, and regulations for medical devices and is recognized as FDA’s expert in the interpretation and application of statutory provisions for medical device exports, remarketed devices, custom devices, and certain postmarket regulatory programs.

He was formerly a Congressional Liaison in FDA's Office of Legislative Affairs and served as a Public Health Advisor in the U.S. House of Representative's Small Business Subcommittee on Regulation, Business Opportunity, and Technology under the LEGIS Fellows Program. He began his FDA career in 1978 as an investigator in Boston, Massachusetts.

Mr. Uldriks has contributed to medical text books concerning FDA’s regulation of medical devices and has been a featured speaker at numerous FDA, professional, and trade association conferences on FDA issues.

He earned his J.D. in 1986 from Suffolk University, his Master of Divinity from Boston University in 1976, and his B.A., cum laude, in 1973 from Albion College. He is admitted to the bars of the Commonwealth of Massachusetts and Federal District Court.