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Medical Device Maker’s Brazen Manipulation of Approval Process Shows Need to Reform FDA
Statement of Peter Lurie, M.D., M.P.H., Deputy Director, Public Citizen’s Health Research Group
In our testimony, we objected to the FDA reviewing the Menaflex under a process less stringent than the more-rigorous Pre-market Approval (PMA) mechanism. In fact, ReGen had initially sought PMA approval but after data collection in its negative, randomized-controlled trial was complete, shifted to the less stringent process. In today’s Wall Street Journal, former FDA Commissioner Andrew von Eschenbach now admits that, "There’s something wrong with how that decision [to use the less stringent process] was made … We fumbled that process." Most patients will never know that the Menaflex reached the market only through the sponsor’s cunning manipulation of the regulatory process, aided and abetted by the FDA, leading to approval through this less-rigorous pathway.
According to the article, ReGen was permitted input into the makeup of the advisory committee, the questions posed to the advisory committee members and who would make the FDA presentation. One is hard-pressed to remember manipulation of an FDA advisory committee so thorough and so brazen.
The article clearly documents the extent to which senior FDA officials are willing to bend over backwards to appease industry, even going so far as to overrule the scientists with most intimate knowledge of the product. Until the agency puts itself back on a secure scientific footing, the public will continue to put little stock in its approval decisions.
READ Public Citizen’s testimony.