#usfda

[halorvic]

[juicetrump2]

US Food and Drug Administration rejects petition to set Pfas limits in food

Environmental protection agency and independent studies have found food biggest source of chemical exposure

[rapeculturerealities]

After Urging From Two Black Congresswomen, FDA Planning To Ban The Harmful Chemicals In Hair Relaxers | Essence

After Urging From Two Black Congresswomen, FDA Planning To Ban The Harmful Chemicals In Hair Relaxers | Essence

U.S. Representatives Ayanna Pressley and Shontel Brown made an inquiry about chemical hair relaxers’ safety earlier this year, prompting the

The U.S. Food and Drug Administration (FDA) is planning to issue a new “proposed rule that would specifically ban hair-straightening products that contain formaldehyde and other formaldehyde-releasing chemicals like methylene or glycol,” CNN reports. And it’s all because of two Black Congresswomen, Representatives Ayanna Pressley Pressley (D-MA) and Shontel Brown (D-OH).

“The F.D.A.’s proposal to ban these harmful chemicals in hair straighteners and relaxers is a win for public health – especially the health of Black women who are disproportionately put at risk by these products as a result of systemic racism and anti-Black hair sentiment,” said Rep. Pressley.

Rep. Brown’s statement was just as effusive, “On behalf of women, especially Black women across the country, I applaud the F.D.A.’s new proposed rule banning formaldehyde and other harmful chemicals from hair straighteners.”

[bestdogfoodforallergies]

Best Dog Food For Allergies in 2021.

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Symptoms of allergies comes via stomach and you can see effected area very easily like on ears, eyes and itchy skin and hair fallen.

Find out more here: best dog food for allergies

[halorvic]

"The FDA this month also suspended existing and developing programs that ensured accurate testing for bird flu in milk and cheese and pathogens like the parasite Cyclospora in other food products. Effective Monday, the agency suspended its proficiency testing program for Grade "A" raw milk and finished products, according to the email sent in the morning from the FDA's Division of Dairy Safety and addressed to "Network Laboratories". Grade "A" milk, or fluid milk, meets the highest sanitary standards. The testing program was suspended because FDA's Moffett Center Proficiency Testing Laboratory, part of its division overseeing food safety, "is no longer able to provide laboratory support for proficiency testing and data analysis," the email said." April 23, 2025

[codresearch]

Streamlining Regulatory Strategy and Pre-Submission Planning

Navigating the complex approvals pathway for novel therapies requires an optimized developmental map that anticipates health authority expectations globally. Incorporating advanced Clinical Development services connects sponsors with dedicated regulatory strategists who analyze your molecular assets proactively. This continuous planning defines your precise regulatory path, facilitating efficient document compilation for initial trial authorizations and ultimate marketing filings.

COD Research serves as an elite operational partner, ensuring your pipelines comply fully with requirements from major international bodies like the USFDA, EMA, MHRA, PMDA, and DCGI. Our specialists provide tailored advice on complex designations—such as Orphan Drug, Fast Track, and Breakthrough Therapy statuses—while mapping out your Pediatric Investigation Plans (PIP). We deliver the compliance intelligence and administrative agility your enterprise needs to secure a faster time to market.

[mavenprofserv]

US FDA 510(k) Consultants: Simplifying Your Regulatory Journey

Bringing a medical device to the U.S. market requires careful planning and compliance with FDA regulations. The 510(k) submission process can be complex, involving predicate device selection, technical documentation, testing, and regulatory review. Working with experienced FDA 510(k) consultants can help manufacturers better understand the requirements and prepare a well-structured submission.

Professional regulatory guidance can support every stage of the process—from identifying the appropriate regulatory pathway to preparing documentation and responding to FDA queries. A strategic approach helps reduce common submission challenges, improve documentation quality, and support a smoother path toward U.S. market entry.

[codresearch]

Clinical Trial Quality Assurance: Global Reach and Regulatory Auditing

Successfully executing multi-center clinical trials across international borders demands deep regional knowledge and consistent quality control protocols. A high-tier Clinical Trial Quality Assurance program provides the global reach necessary to manage complex regulatory inspections across varied administrative landscapes. This includes conducting rigorous site audits and protocol health checks to identify and resolve compliance discrepancies before formal agency evaluations begin.

COD Research brings extensive operational experience to your research portfolio, successfully managing regulatory inspections from major international health bodies. Our auditors possess deep insight into global compliance expectations, including guidelines set forth by the USFDA, EMA, MHRA, ANVISA, and regional authorities like the DCGI. We provide the thorough technical oversight and protective risk management required to guide your molecule smoothly through international approval pathways.