Military service comes with life-threatening risks, but a study published in November 2019 shows that tens of thousands of veterans are dying from an invisible danger: air pollution in the U.S. The researchers concluded that the EPA standards for air quality are not adequate to protect Americans from death caused by air pollution, and their […]
Read More »Medical Care for Adults
The National Center for Health Research reviews important new research as soon as it is published. We cut through the hype regarding various medical treatments to let you know what is proven and what is unknown about the risks and benefits of various treatment options. We do not accept funding from the companies that make medical products, so you can trust that our information is based on science, and not biased by financial ties to the treatments we’re evaluating.
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NCHR Comments on Adverse Events Program for Medical Devices, Medical Product Safety Network (“MedSun”)
June 23, 2017. The FDA must improve post-market surveillance of medical devices, and MedSun should be part of that effort.
Read More »NCHR Comments on FDA’s Notice on the Modified Risk Tobacco Product Application for Copenhagen Snuff Fine Cut
January 21, 2020. We strongly oppose the approval of the modified risk application for Copenhagen Snuff Fine Cut with the claim “IF YOU SMOKE, CONSIDER THIS: Switching completely to this product from cigarettes reduces risk of lung cancer.” This claim may encourage non-smokers to begin using tobacco. Using smokeless tobacco increases the risk of serious health issues.
Read More »How Safe is CBD?
Cannabidiol (CBD) is an ingredient in cannabis and hemp that has taken the public by storm. But is CBD safe? There is currently no concrete, scientific evidence of its benefits besides treating pediatric epilepsy.
Read More »Roundup 2019: Breast implants, mesh, paclitaxel-coated devices among hot topics at FDA expert panels
MedTech Dive, December 23, 2019. As the FDA approves medical devices, it is essential that the public is made aware of inadequate post-approval studies and spotty adverse event reporting.
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