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We’re Speaking Out on Health Issues

NCHR scientists and health policy experts provide written and oral statements on a wide range of topics.

Here are many of the ways we have been Speaking Out on Health Policy Issues for the last few years.  Whether the topic is legislation intended to cure diseases, proposed bans on BPA or other chemicals that disrupt your hormones, the importance of including women, people of color, and patients over 65 in clinical trials, or many other topics, you’ll gain a better understanding of our evidence-based analyses by reading these letters, statements, and testimony.

Here are the ways we have been Speaking out on Medical Treatments and Products, such as prescription drugs and medical devices that the FDA is considering approving, or is considering taking off the market because of serious risks.  Whether the topic is Chantix, Addyi, Yaz, Essure, or medical products you’ve never heard of, you can find out more about what is known and not known about the safety and effectiveness of a wide range of products by looking through this section of our website.

NCHR Testimony to FDA in Preparation for the 2017 International Cooperation on Cosmetics Regulation (ICCR) Meeting

Megan Polanin, May 25 2017: The National Center for Health Research is asking the FDA and international cosmetic regulators to take action on harmful chemicals in beauty products. They point out that substances like phthalates and parabens, found in everyday items like lotions and toothpaste, can affect hormones and may harm children’s development.

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NCHR Testimony to FDA About L-Glutamine for Sickle Cell Crisis

Stephanie Fox-Rowlings May 24 2017: FDA should only approve new treatments when there is clear proof they are safe and helpful. If many people drop out of the study, it’s hard to know if the drug really works, and the FDA should not approve it without strong evidence.

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NCHR Testimony to FDA About Neratinib to Prevent Breast Cancer Reccurance

The National Center for Health Research advises the FDA to delay approval of neratinib for early-stage HER2-positive breast cancer, highlighting that the drug offers only a slight improvement in preventing cancer recurrence while causing serious side effects like severe diarrhea and fatigue, which led many patients to stop treatment.

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Nonprofit Groups’ Letter to Secretary Price on the Tobacco “Deeming Rule”

May 17, 2017. In light of the overwhelming record evidence compiled by the FDA, there is no public health justification for the FDA to reconsider the deeming rule, or to postpone the implementation of its provisions.

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Coalition Letter Supporting Smoke-Free VA Facilities

May 11, 2017. We write in support of H.R. 1662, which would make facilities of the Veterans Health Administration (VHA) smoke-free.

Read More »
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