https://www.eenews.net/articles/house-dems-press-fda-on-formaldehyde-ban-delay/
House Dems press FDA on formaldehyde ban delay - E&E News by POLITICO
Aug 30, 2024 - The agency blew past two earlier deadlines for finalizing a prohibition on formaldehyde in hair-straightening products.
fda on
https://www.bio.org/letters-testimony-comments/bio-comments-fda-their-advanced-manufacturing-technologies-designation
BIO Comments to FDA on their Advanced Manufacturing Technologies Designation Program | BIO
The Biotechnology Innovation Organization (BIO) thanks the Food and Drug Administration (FDA) for the opportunity to submit comments regarding the request and...
fda onadvanced manufacturingbiocomments
https://www.tmj4.com/news/addictive-drug-or-alternative-to-break-the-habit-doctors-dispute-fda-about-effects-of-kratom
Doctors challenge FDA on effects of Kratom
Mar 14, 2018 - Is it an addictive drug, or a way to actually overcome addiction? The FDA is considering regulating an herbal drug called Kratom. But a group of doctors is...
fda ondoctorschallengeeffectskratom
https://www.ttnews.com/articles/industry-groups-wary-plan-fda-food-transport
Industry Groups Wary of Plan from FDA on Food Transport - TT
Aug 31, 2022 - Trade groups representing the food, shipping and trucking industries have voiced caution and opposition to a plan by the U.S. Food and Drug Administration to...
industry groupsof planfda onfood transportwary
https://ific.org/insights/ific-foundation-comments-to-fda-on-alternate-name-for-potassium-chloride/
IFIC Foundation Submitted Comments to FDA on Alternate Name for Potassium Chloride - IFIC
Sep 10, 2025 - The Food and Drug Administration (FDA) has issued draft guidance regarding the use of an alternate name for potassium chloride in food labeling. The...
fda on
https://www.acr.org/News-and-Publications/acr-provides-input-to-fda-on-ai-measurement-and-evaluation
ACR Provides Input to FDA on AI Measurement and Evaluation
ACR submitted comments to FDA on real-world AI device performance, stressing safety, governance, and continuous monitoring.
fda onai measurementacrprovidesinput
https://www.citizen.org/article/letter-to-fda-on-the-case-of-upjohn-and-halcion/
Letter to FDA on the case of Upjohn and Halcion - Public Citizen
on the caseletter to
https://asm.org/articles/policy/2026/april/asm-responds-to-fda-on-dietary-supplement-ingredie
ASM Responds to FDA on Dietary Supplement Ingredients
ASM responds to a request for public comment from the Food and Drug Administration on the scope of dietary supplement ingredients.
fda ondietary supplementasmrespondsingredients
https://www.citizen.org/article/letter-to-fda-on-criminal-prosecution-of-the-upjohn-company/
Letter to FDA on Criminal Prosecution of the Upjohn Company - Public Citizen
the upjohn companyletter tofda oncriminal prosecution
https://www.fda.gov/food/food-safety-modernization-act-fsma/fsma-final-rule-requirements-additional-traceability-records-certain-foods
FSMA Final Rule on Requirements for Additional Traceability Records for Certain Foods | FDA
The final rule aligns with current industry best practices and covers domestic, as well as foreign firms producing food for U.S. consumption, along the entire...
final rule