Rep. Henry Waxman (D-Calif.) is urging the FDA not to release a guidance allowing drug and medical device companies to use journal articles to promote off-label use of their products.
Waxman recently released a copy of the draft guidance, which has not yet been issued by the agency, and sent a letter to the FDA requesting that it not continue work on the document until it provides further information to the House Oversight and Government Reform Committee.
According to the guidance, if a manufacturer were to follow the agency’s recommendations and there were no unlawful promotion of the manufacturer’s product, the FDA would not view the distribution of medical and scientific information as evidence of manufacturer intent that the product can be used for an unapproved use.
Waxman said a fundamental tenet of drug and device law is that a manufacturer cannot market a drug or device for a therapeutic use without FDA approval. The draft guidance “would carve a large loophole in the law,” allowing manufacturers to promote off-label uses of their products by passing out journal articles about those uses to physicians, he said.