About Michael A. Swit, Esq.
Navigating successfully the maze of  legal and regulatory requirements
governing pharmaceuticals, biologics, medical devices and other
FDA-regulated products requires experienced, well-honed insights and
understanding of both the bounds of the law and agency policy...
Michael Swit has been addressing critical FDA legal and regulatory issues since 1984.  Before joining Duane
Morris LLP as a Special Counsel in its San Diego office in March 2012, Mr. Swit served for seven years as a
Vice President for The Weinberg Group, a premier FDA regulatory consulting firm headquartered in
Washington, D.C., where he developed and ensured execution of a broad array of regulatory and other
strategies, compliance and enforcement initiatives, recalls and crisis management, submissions and related
traditional FDA regulatory activities, labeling and advertising, and clinical research efforts for drug, biologic,
device, IVD, and other life sciences companies, as well as those in the food, cosmetic, and dietary supplement
industries.

Mr. Swit's multi-faceted experience includes serving for three and a half years as corporate vice president and
general counsel of Par Pharmaceutical, a major publicly-traded generic drug manufacturer and, thus, he brings
an industry and commercial perspective to his work with FDA-regulated companies.  While at Par, he
spearheaded Par's successful response to multiple federal and state criminal and civil investigations arising out
of the actions of prior management.  Mr. Swit then served for over four years as CEO of FDAnews.com, a premier
publisher of FDA regulatory newsletters and other specialty information products for the FDA-regulated
community.

His private FDA regulatory law practice has included service as Special Counsel in the FDA Law Practice Group
in the San Diego office of Heller Ehrman White & McAuliffe and with the Food & Drug Law practice at
McKenna & Cuneo, both in the firm's Washington office and later in San Diego.  He also has been a solo FDA
law practitioner.  He first practiced FDA regulatory law with the D.C. office of Burditt Bowles & Radzius.  

Mr. Swit has taught and written on a wide variety of subjects relating to FDA law, regulation and related
commercial activities, including, since 1989, co-directing a three-day intensive course on the generic drug
approval process and editing a guide to the generic drug approval process,
Getting Your Generic Drug Approved. A
former member of the
Food & Drug Law Journal Editorial Board, Mr. Swit also has been a prominent speaker at
numerous conferences sponsored by such organizations as RAPS, FDLI, and DIA.

A
magna cum laude graduate of Bowdoin College, with high honors in history, Mr. Swit received his law degree
from Emory University School of Law.  He is a member of the California Bar and was admitted previously in
both Virginia and the District of Columbia, but is not currently active in either jurisdiction.

Mr. Swit is also an avid cyclist and hockey, basketball and baseball fan, and the father of
triplet sons, born on
Leap Day, Feb. 29, 1996.


To view Mr. Swit's biography on the Duane Morris website, click here ...                    

          Follow on LinkedIn:  
http://www.linkedin.com/in/michaelswit
                  Follow on Twitter:  https://twitter.com/FDACounsel
For a copy of
Mr. Swit's full
CV
, click here ...
© 2014   Michael A. Swit.  
ALL RIGHTS RESERVED.

Questions?

Contact me @ 760-815-4762
or
mswit@fdacounsel.com
Michael A. Swit