Agency is accepting contractor proposals through August 11 for a scientific literature survey and data analysis to determine whether 25 cosmetic ingredients/mixtures warrant identification as “sensitizers” or “allergens,” according to definitions being developed separately. Preservatives dominate the list.
FDA is soliciting proposals for contract research to assess the allergenicity and sensitization potential of 25 cosmetic ingredients/mixtures – mostly preservatives – based on published scientific data and consensus-backed definitions.
“In order to develop a regulatory position that is based on the most relevant scientific literature, the FDA needs a...
Devices authorized for marketing outside the US. Data derived from Citeline’s Meddevicetracker. Updated weekly.
PATIENT ACCESS TO UNAPPROVED MEDICAL PRODUCTS WOULD BE ALLOWED under legislation introduced by Rep. Peter DeFazio (D-Ore.) on July 12 and Sen. Tom Daschle (D-S.D.) on July 14. Called the Access to Medical Treatment Act, the legislation would allow health practitioners to administer unapproved drugs, devices, foods or dietary supplements to patients as long as there is no evidence the treatment causes harm and the patient is informed about the treatment and its possible side effects. DeFazio's bill is identified as HR 2019; Daschle's version will be assigned a bill number the week of July 17.
A look at new research on the cardiovascular effects of ADHD medications and what it means for clinical care. This article explores the latest clinical and epidemiological research on the cardiovascular effects of medications commonly prescribed for ADHD, examining potential heart-related risks, underlying mechanisms, and their implications for patient safety, clinical decision-making, and long-term treatment strategies across diverse age groups and risk profiles.
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