U.S. FDA

The FDA is releasing the Regulatory Accelerator, a set of resources that support FDA’s priority to accelerate cures and treatments by helping digital health innovators bring safe and effective medical devices to market. fda.gov/medical-device…

The FDA is advising consumers not to eat & restaurants & food retailers not to serve or sell & to dispose of these frozen, raw, half-shell oysters that were shipped to distributors in AZ, CA, CO, MT & UT, & may have been distributed to other states as well fda.gov/food/alerts-ad…

Recalled Ready-to-Eat (RTE) foods are past shelf life and are no longer available for sale. fda.gov/food/outbreaks… CDC has declared the outbreak over & FDA’s investigation is complete.

Dozens of scientific studies have found links between the consumption of foods often considered ultra-processed with numerous adverse health outcomes. HHS and @US_FDA are working with @USDA to establish a federally recognized uniform definition for ultra-processed foods—a…

.@DrMakaryFDA and @DrOzCMS just delivered landmark victories for the American People. MAHA is winning, not through blunt-force regulation, but by working with industry.

You win more bees with honey than with fire. Check out my op-ed with @DrOzCMS about how MAHA is driving meaningful change by using our convening power and calling on industry leaders directly. Everyone wins when the government leads with purpose instead of paperwork.…

The FDA is announcing a forthcoming public advisory committee meeting of the General and Plastic Surgery Devices Panel of the Medical Devices Advisory Committee (the Committee). For more information, please visit: fda.gov/advisory-commi…

Women live longer and feel better when they start Hormone Replacement Therapy within 10 years of the onset of menopause. Every woman needs to know about this and watch our FDA expert panel that just took place. @Morning_Joe

Consumer Brands Association joins the growing list of U.S. food and beverage producers committed to removing petroleum-based food dyes. fda.gov/news-events/pr…

Companies aligned with U.S. national priorities can now submit statements of interest for participation in the Commissioner’s National Priority Voucher (CNPV) pilot program. Statements of interest are capped at 350 words! More details here: FDA.gov/CNPV

In this FDA Direct, @DrMakaryFDA welcomes FDA’s new Director of the Center for Drug Evaluation and Research, Dr. George Tidmarsh. Dr. Tidmarsh brings more than 30 years of experience spanning biotechnology, clinical medicine, and regulatory science, and will lead FDA’s efforts to…

STREAMING LIVE - Stanford Physician-Scientist, Swimmer, Inventor: FDA welcomes George Tidmarsh, M.D., Ph.D. as Director of CDER youtube.com/live/rOdAzhnSa…

LIVESTREAMING NOW: FDA Expert Panel on Selective Serotonin Reuptake Inhibitors (SSRIs) and Pregnancy