Casper "Cap" Uldriks

Casper “Cap” Uldriks brings over 32 years of experience from the FDA.  As a field investigator, he conducted import operations in the New England (Boston) District Office, which provides broad-based practical knowledge of FDA’s import program and procedures.  As a senior manager in the Office of Compliance and as an associate center director for the Center of Devices and Radiological Health (CDRH), he served as the center’s expert on import and export operations and policy.

He managed the implementation of the FDA Export Reform and Enhancement Act of 1996 and development of intra-agency policy for imports, exports, and entry criteria for the FDA’s risk-based software screening program, known as PREDIDT. He routinely trained FDA staff and was featured as a public speaker on the statutory import and export requirements and how they operated for enforcement purposes. He is recognized as an engaging and energetic speaker.  His comments are candid, straightforward, and of practical value.  He understands how FDA thinks and operates, and where it is headed.

Courses Taught