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Kathleen M. Sanzo, Partner
- 202-739-5209
- ksanzo@morganlewis.com
- www.morganlewis.com
Kathleen M. Sanzo is a partner in and leader of Morgan Lewis's FDA and Healthcare Practice. Ms. Sanzo's practice focuses on all regulatory and compliance matters of the Food and Drug Administration relating to bulk and finished prescription and OTC drug and biologic manufacture, approval, marketing, and distribution; pre-clinical and clinical testing; drug and device promotional and labeling issues; food additive and dietary supplement matters; state and federal privacy regulatory and compliance issues; healthcare regulatory and enforcement matters of the Office of Inspector General of the Department of Health and Human Services and the Centers for Medicare and Medicaid Services; and regulatory and compliance matters of the Consumer Product Safety Commission and related state enforcement agencies.
- Morgan, Lewis & Bockius LLP
Articles in the National Law Review database by Kathleen M. Sanzo:
- FDA Issues Three Draft Guidances for Biosimilars (Posted On Friday, February 10, 2012)
- FDA Requests Comments on the Development of a User Fee Program for Biosimilar and Interchangeable Biological Products (Posted On Tuesday, May 24, 2011)
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