From: Judith Miller [paradisegds@yahoo.com]
Sent: Sunday, March 25, 2001 9:19 PM
To: fdadockets@oc.fda.gov
Subject: docket 00N-1396 & docket 00D-1598

Haven't you folks learned anything from the mad cow
disease problem?
Unrestrained factory agriculture is what caused it.

Regarding your dockets listed in the subject line:
The FDA must require mandatory pre-market
comprehensive environmental review.

The FDA must require mandatory pre-market long-term
health testing. GE products could be toxic, cause
allergic responses, have lower nutritional value, and
compromise immune responses in consumers.

The FDA must require mandatory labeling of GE
products.  I HAVE THE RIGHT TO SAY NO TO FOOD I DON'T
WANT TO EAT!!!!!!!!!!!!!! 
  Without mandatory labeling, neither consumers nor
health professionals will know if an allergic or toxic
reaction was the result of a genetically engineered
food.  TRYING TO MAKE AN END-RUN AROUND LAWSUITS, ARE
YOU?
* The FDA must end its cozy relationship with the
industries it purports to be regulating. 
DAMN STRAIGHT!!!!
People have been allowed to work for a biotech
company, then work for the FDA writing the regulatory
rules on that company's product, then go back to
oworking for the company.  Ninety-two percent of FDA
advisory committee meetings had at least one conflict
of interest.
HOW ABOUT PROTECTING THE CONSUMER FOR A CHANGE?
Judith Miller
paradisegds@yahoo.com


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