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Re: Powerful FDA testimony re: labelling GE foods
Marcus--
Steven Drucker's testimony was presented at the second of three public
hearings the FDA held in November and December. The first was a
"surprise" in Chicago, we found out at the eleventh hour. The FDA
provided 150 seats--the midwest grain capital, millions of people live
in the metro area--150 seats for a PUBLIC hearing! Monsanto knew about
it. After a phone call barrage, a new space to accommodate more people
was located. Guess the FDA thought no one would pay attention. We did,
but for many people in the midwest, it was too late for them to come.
The second hearing, held November 30 in Washington DC was scheduled the
same time as WTO. It got lost too (whoops! so sorry, poor planning). The
third and final public hearing was held in Oakland, California.
The FDA says they want to hear from US citizens about this issue,
specifically labeling. We have until January 13 (some sources say the
16th) to make a statement. Call, write or e-mail the FDA Commissioner to
voice your concerns:
Dr. Jane E. Henney, Commissioner, Food and Drug Administration, Dockets
Management Branch H-F 305, 5603 Fishers Lane, Room1061, Rockville, MD
20852, Docket #99N-4282 . (301) 827-2410. e-mail: execsec@oc.fda.gov;
Comments may be submitted via the FDA web site at
www.fda.gov/ohrms/dockets. Identify docket number on correspondence.
Drucker's testimony may be accessed at:
http://www.biointegrity.org
You may reach him for permission to publish on your website through
BioIntegrity, located in Iowa, he's the director of the organization and
they are currently involved in a lawsuit with the FDA. This site also
holds scanned internal FDA documents, now public documents.
Controversial, browse these docs, make up your own mind.
>
> "Why Food & Drug Administration Policy on Genetically Engineered Food
> Violates Sound Science & U.S. Law"
>
> PRESENTATION of STEVEN M. DRUKER, J.D., Executive Director of the
> Alliance for Bio-Integrity, AT THE FDA PUBLIC MEETING ON GENETICALLY
> ENGINEERED FOODS, NOV. 30, 1999,WASHINGTON, D.C. Panel on Scientific,
> Safety, and Regulatory Issues
>
> A. Introduction : I am very pleased to be here, and I commend you,
> Commissioner Henney, for holding these meetings. I am also somewhat
> surprised to be here, since I am one of the stro
>
entire testimony at: http://www.biointegrity.org/fdaPMP.html
Peace,
Donna