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Biofield Corp. Reinitiates FDA Review Process For Detection Device.(Biofield Diagnostic System)

Women's Health Weekly

| November 01, 2001 | COPYRIGHT 2001 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2001 OCT 25 - (NewsRx.com & NewsRx.net) -- Biofield Corp. (BZET) met with the U.S. Food and Drug Administration (FDA) on September 10, 2001, as the first step in reinitiating its application for approval of its Biofield Diagnostic System (BDS). The BDS is designed to measure the electrical changes in cells as they divide, and to identify those dividing abnormally, such as cancer cells.

During the meeting, Biofield discussed data it had obtained on more than 1500 women analyzed for breast cancer with the BDS. The patient data discussed with the FDA, including those checked for accuracy against monoclonal antibodies for the assessment of proliferating cells, will be used in an updated Biofield application to the FDA. This action initiates another step toward approval of the BDS for commercialization within the United States. The BDS has a CE Marking to enable it to be sold ...

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Source: HighBeam Research, Biofield Corp. Reinitiates FDA Review Process For Detection...

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