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M. Elizabeth Bierman, Partner
- 202-739-5206
- mebierman@morganlewis.com
- www.morganlewis.com
M. Elizabeth Bierman is a partner in Morgan Lewis's FDA and Healthcare Practice. Ms. Bierman has more than 20 years of experience in representing domestic and international companies with respect to all FDA regulatory and compliance matters relating to the development, manufacturing, and marketing of medical devices, pharmaceuticals, biologicals, combination products, medical foods, and infant formulas.
- Morgan, Lewis & Bockius LLP
Articles in the National Law Review database by M. Elizabeth Bierman:
- FDA Issues Draft Guidance on 510(k) Device Modifications: New Emphasis on Potential Impact of Modifications (Posted On Wednesday, August 10, 2011)
- New FDA Draft Guidance on Mobile Medical Apps Provides Some Clarity, But Raises Many More Questions (Posted On Tuesday, August 2, 2011)
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