Bullous Pemphigoid

FDA Clears MBL Bullous Pemphigoid ELISA Test

Published in Medical Letter on the CDC and FDA, October 12th, 2008

MBL International Corporation of Woburn, Massachusetts is announcing that the United States Food and Drug Administration, FDA, has cleared the BP180 and BP230 ELISA Kits for the detection of Bullous Pemphigoid (BP), the new kits have been CE marked as well. The new kits are seen as an advance in diagnosing Bullous Pemphigoid.

MBLI's Chief Executive Officer Dennis Walczewski, was pleased to offer this new medical advance and was quoted as saying, "These new kits present a significant advance in testing for this irritating skin malady and it is our hope that improved testing can lead to better treatment."

Bullous Pemphigoid, which is an autoimmune...

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Source: Medical Letter on the CDC and FDA (2008-10-12)

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