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51st Food and Drug Law Institute Annual Conference Focuses on Relationship Between Scientific Advances and FDA Law & Regulation
Date:1/9/2008

e General Counsel, Food & Drug Division, Department of Health & Human Services;

Daniel Meron, General Counsel, Department of Health and Human Services;

Thomas Miller, Member, Managing Board, Siemens Medical Solutions;

Paula A. Monopoli, Professor, University of Maryland School of Law & Founding Director, Women, Leadership & Equality Program;

Lydia Parnes, Director, Office of Consumer Protection, Federal Trade Commission;

David Schmidt, President & CEO, International Food Information Council;

Barry M. Straube, M.D., Chief Medical Officer, Center for Medicare & Medicaid Services;

Daniel E. Troy, Partner, Sidley Austin;

Janet Woodcock, M.D., Deputy Commissioner and Chief Medical Officer, FDA; and

Julie Zawisza, Assistant Commissioner for Public Affairs, FDA.

For a complete list of speakers and agenda, visit http://www.fdli.org.

The Early Bird Rates, effective through Feb. 15, are:

Both One Day

Days Only

$945 $795 FDLI Members

$1,270 $1,020 Non-members

$395 $345 Government (Non-FDA, including FDAAA members who

are not currently employed)

$670 $470 Academics, 501(c)(3) Non-Profits

$399 $199 Full Time Students (Special discount: $350 for a

group of 5 or more who register for both days)

To register for the conference, visit http://www.fdli.org or call (800)956-6923 or (202) 371-1420.

Founded in 1949, FDLI publishes the award-winning, peer-reviewed Food and Drug Law Journal; the bimonthly magazine Update; FDA Directory; and dozens of books and publications for attorneys, regulatory affairs practitioners, scientists, health care professionals, government employees
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