Just How Broken is the FDA?
The reexamination of a knee device and a campaign to extend the patent of a blood-thinning medication underscore the need for FDA reform.
The reexamination of a knee device and a campaign to extend the patent of a blood-thinning medication underscore the need for FDA reform.
Each week brings new studies confirming the benefits of vitamin D, and yet there is widespread vitamin-D deficiency in industrialized nations. Why is the government standing in the way of our addressing this public-health crisis?
Despite beginning a process to retract their previous assertion that BPA (bisphenol A) is safe, the FDA claims to be “powerless to regulate BPA.” Give us a break!
The University of California, Davis, recommends boosting your vitamin D intake during the winter months by a factor of 5!
The FDA’s failure to protect newborns and the unborn from BPA recalls the old joke “How many deaths does it take for the FDA to remove a drug from the market?” The answer (not all funny): all too many.
The Center for Science in the Public Interest (CSPI) has asked the Food and Drug Administration (FDA) to abolish Structure/Function Claims and Qualified Health Claims. What does this jargon mean? Why is this so important?
The Natural Products Association (NPA) and the Council for Responsible Nutrition (CRN) have both voiced outrage over the publication of “Cancer Incidence and Mortality after Treatment with Folic Acid and Vitamin B12” in the 11/19/09 issue of JAMA.
All children deserve the best protection we can provide, but the government is failing to shield our most vulnerable population — the unborn — from chemicals in the environment.
Nine French lawmakers, citing the ban by Canada and a number of U.S. states, have proposed legislation to ban bisphenol A (BPA) in all food containers (including baby bottles) setting the stage for France to become the first European country to ban BPA. In May, Denmark’s parliament passed a resolution calling on its government to […]
Legislation unanimously passed the House of Representatives this month that would recognize hyperbaric oxygen therapy (HBOT) in Veterans Administration medical facilities across the country and report the results to Congress. Rep. Pete Sessions (R–TX) authored the legislation as an amendment to the 2010 fiscal year Military Construction and VA Appropriations Act. The new legislation requires […]