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Deborah C. Attwood

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Washington,  DC  U.S.A.
Phone202.434.4107

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Experience & Credentials
 

Practice Areas

  • Food & Drug
     
    University Boston University, B.A., magna cum laude, 2004
     
    Law SchoolGeorge Washington University Law School, J.D., 2009
     
    Admitted2009, Virginia; 2010, District of Columbia
     
    Biography

    Deborah Attwood joined Keller and Heckman in 2009. She practices in the area of food and drug law. In particular, Ms. Attwood advises both domestic and international clients on product compliance with FDA regulations pertaining to direct and indirect food additives, food packaging, and labeling issues.

    While attending The George Washington University Law School, Ms. Attwood clerked for the U.S. Environmental Protection Agency Office of Enforcement and Compliance Assurance, U.S. Department of the Interior Office of the Solicitor, and the non-profit organization Oceana. Ms. Attwood also participated in various pro bono activities, including testifying before the D.C. Council regarding pending legislation. Prior to law school, Ms. Attwood was a paralegal for a law firm in Boston, Massachusetts, and specialized in defending against toxic tort litigation.

    News, Events & Articles

    News

    Dec 07, 2011, David Ettinger and Deborah Attwood Co-Author Feature Article in FDLI's November/December Update

    Jun 10, 2011, Keller and Heckman Attends FDA Public Meeting on FSMA Inspections and Compliance Provisions

    Jun 06, 2011, Partner Mel Drozen and Associate Deborah Attwood to Attend FDA's Public Meeting

    Articles

    Mar 13, 2012, FDA Publishes Criteria for "High Risk" Facilities

    FDA Continues FSMA Implementation For User Fees and Suspension of Registration

     
    ISLN921467418
     

    Documents by this lawyer on Martindale.com

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    FDA Issues Two Draft Guidances on Nanotechnology
    Deborah C. Attwood,Melvin S. Drozen,Laura C. Foley, May 4, 2012
    On April 20, the U.S. Food and Drug Administration (FDA) released two draft guidance documents primarily focused on the use of nanotechnology by the food and cosmetics industries. The two guidance documents are "Guidance for Industry: Assessing the Effects of Significant Manufacturing Process...

    FDA Publishes Criteria for "High Risk" Facilities
    Deborah C. Attwood,Melvin S. Drozen, March 16, 2012
    On March 9, 2012, the Food and Drug Administration (FDA) published on its website "FSMA Domestic Facility Risk Categorization (FY 2012)," identifying the criteria FDA uses when categorizing "high risk" domestic facilities that are subject to more frequent FDA inspections, as...

    FDA Continues FSMA Implementation For User Fees and Suspension of Registration
    Deborah Attwood,Melvin S. Drozen,Evangelia Cadenas Pelonis, August 5, 2011
    The Food and Drug Administration (FDA) is continuing its efforts to implement the FDA Food Safety Modernization Act in accordance with required deadlines. On Monday, August 1, FDA published a Federal Register Notice announcing the fiscal year (FY) 2012 fee schedule for certain domestic and foreign...
    Profile Visibility
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    Office Information

    Deborah C. Attwood
    Keller and Heckman LLP
    Suite 500 West, 1001 G Street, N.W.
    Washington, DC 20001




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