Guest guest Posted October 25, 2008 Report Share Posted October 25, 2008 http://www.usatoday.com/news/health/2008-10-24-bpa-congress-fda_N.htm A rubber duck sits on the desk of Rep. Jan Schakowsky, D-Ill., during a June Capitol Hill hearing of the House Commerce, Trade and Consumer Protection subcommittee on the safety of phthalates and BPA in consumer products. Congress questions FDA objectivity on BPA plastic safety By Liz Szabo, USA TODAY Oct 24, 2008 Congress is stepping in to ask questions about chemical industry influence in drafting a Food and Drug Administration report about the safety of a controversial chemical in baby bottles. In August, the FDA declared the chemical, bisphenol A, or BPA, safe, a determination greeted skeptically by consumer groups who argue that hundreds of scientific studies suggest it may cause serious harm. According to a letter to the FDA from Reps. Dingell and Bart Stupak sent last week, the FDA hired a private consulting group with strong industry ties to perform some of its analyses of BPA. Work performed by Virginia-based ICF International "formed the basis for the draft," says Jodi Seth, a spokeswoman for the House of Representatives' Committee on Energy and Commerce, which Dingell chairs. Sen. Grassley, R-Iowa, also wants to know exactly who wrote the FDA report. In a letter to the FDA last month, Grassley pointed out that the report appears to be anonymous. He has written to FDA Commissioner von Eschenbach to supply him with the names of everyone who worked on it. Both Democrats and Republicans have questioned why the FDA used only industry-funded research when determining that BPA is safe. And Dingell and Stupak, both Michigan Democrats, note that the chairman of an FDA advisory panel on BPA heads a research center that accepted a $5 million gift from a retired medical device manufacturer who says the chemical is safe. That expert panel, a subcommittee of the FDA's larger Science Board, has been asked to provide an outside review of the BPA report. Given the potential for bias, the FDA should require the panel chairman, Philbert of the University of Michigan , to return the $5 million or withdraw from the panel, Rep. Markey, D-Mass., wrote in a separate letter. In an interview, Philbert says his research money has come entirely from federal grants and the W.M. Keck Foundation. Philbert says he has given lengthy descriptions of all potential conflicts to the FDA, and that the agency has reviewed these materials three times. The FDA has not asked him to step down, however, and Philbert says he plans to continue volunteering on the subcommittee. Philbert says he has never discussed BPA with the donor, Gelman. When Gelman began to raise the subject during one conversation, Philbert says he immediately changed the subject. "I have serious concerns about this agency's ability to protect our children from a potentially dangerous chemical," Stupak said in a statement. Grassley also has asked why the FDA has ignored research funded by taxpayers through the National Institutes of Health. He notes that the FDA appears to be using a different standard than the National Toxicology Program — part of the Department of Health and Human Services — which relied on government-funded research to conclude there is "some concern" that BPA may affect development of the brain, behavior and prostate in children exposed before and after birth. And Grassley notes that scientists are finding additional evidence of BPA's dangers all the time. Just last month, he notes, researchers writing in the Journal of the American Medical Association linked BPA to heart disease and diabetes in adults. Lindsey Litton, a spokeswoman for ICF International, says its contract with the FDA doesn't allow her to discuss the company's work. But she says that ICF works on hundreds of contracts a year, both for business and government. "The conduct of all of these projects is governed by strict conflict of interest and ethics policies to ensure that our objectivity and integrity is maintained at all times," she says.University of Michigan spokeswoman Cunningham says Philbert, who leads the the University of Michigan Risk Science Center, has no conflict of interest. The donation was made to the university, rather than to him, Cunningham says. Philbert's salary doesn't come from the donation or from the center. A spokesman for the FDA declined to comment, noting that the agency is preparing answers to lawmakers' questions. The advisory panel is scheduled to release its review of the FDA's report on BPA before it meets Oct. 31. The panel will present its findings to the FDA's Science Board, which may issue its own assessment of the agency's work. A growing number of retailers, manufacturers and government officials are taking action against BPA. Canada last week declared BPA to be toxic and announced plans to ban it in baby bottles. Markey has introduced legislation to ban BPA in food and beverage packaging. Attorneys general from Connecticut , New Jersey and Delaware have asked 11 companies to stop using BPA in baby bottles and formula cans. In response to Dingell and Stupak's investigation, major baby formula manufacturers have said they are working to take BPA out of the linings of their liquid formula cans. Most baby bottle makers also now offer BPA-free alternatives. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.