Product Identification for Life Sciences

Medical Device UDI Requirements (FDA and EU)
Pharmaceutical – Serialization, e-Pedigree and Track and Trace (EU, China, California, Brazil, etc.)

New regulatory deadlines will shortly affect Life Sciences companies distributing products in the U.S. EU and many parts of Asia and South America. The regulatory deadlines are such that immediate assessment of your company strategy; clear definition of your program; and aggressive implementation are required. USDM’s Governance Risk and Compliance Practice and UDI team provides offerings to enable life sciences organizations to successfully define and execute all levels of the programs.



  • Clintrak - Jeffrey D. Coffin
    I have had the great pleasure to work with Bob for 5 years in his position of VP of Quality at Fisher Packaging Services while I acted as Director of Quality services at a sister…
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