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FDA Counterfeit Drug Task Force -- 2006

Co-Chairs:

Margaret Glavin
Associate Commissioner for Regulatory Affairs
Office of Regulatory Affairs

Randall Lutter, Ph.D.
Associate Commissioner for Policy and Planning
Office of the Commissioner

Task Force Members:

Deborah Autor, Esq.
Associate Director, Office of Compliance
Center for Drug Evaluation and Research

Jane Axelrad, Esq.
Associate Director for Policy
Center for Drug Evaluation and Research

Carolyn Becker, Esq.
Regulatory Counsel
Office of Regulatory Affairs

Ilisa Bernstein, Pharm.D., J.D.
Director of Pharmacy Affairs
Office of the Commissioner

Randy Levin, M.D.
Associate Director for Medical Informatics
Center for Drug Evaluation and Research

William McConagha, Esq.
Associate General Counsel
Office of the General Counsel

Moheb Nasr, Ph.D.
Director, Office of New Drug Quality Assessment
Center for Drug Evaluation and Research

Steve Niedelman, Esq.
Deputy for Regulatory Operations
Office of Regulatory Affairs

Jeff Shuren, M.D., J.D.
Assistant Commissioner for Policy
Office of the Commissioner

Steve Silverman, Esq.
Acting Deputy Director, Office of Compliance
Center for Drug Evaluation and Research

Robert Sausville
Acting Deputy Director, Office of Compliance and Biologics Quality
Center for Biologics Evaluation and Research

Toni Stifano
Special Assistant, Office of Compliance and Biologics Quality
Center for Biologics Evaluation and Research

Terry Vermillion
Director, Office of Criminal Investigations
Office of Regulatory Affairs

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