FDA warns ‘Dr. Goodenowe’ health centre founder that his recent supplement study put patient health at risk

The U.S. Food and Drug Administration (FDA) has rebuked the founder of Moose Jaw’s controversial Dr. Goodenowe Restorative ...

As Healthcare AI Changes On The Fly, FDA Reconsiders How To Keep It Safe

The FDA's approval process was designed for medical devices that stay largely the same after launch. Clinical AI does not operate this way; it is built to evolve.
JD Supra

What FDA’s TEMPO Pilot and CMS’s ACCESS Model Mean for Medical Device Manufacturers

The U.S. Food and Drug Administration (FDA) and the Centers for Medicare & Medicaid Services (CMS) have launched two coordinated initiatives: the ...

A Key Pharmaceutical Equipment Manufacturer Upholding Global Health Supply Chain Integrity

The pharmaceutical industry operates under an uncompromising mandate: zero defects. Every tablet, capsule, vial, or syringe must meet exacting standards for dosage, purity, and sterility. This ...

Top New Material Manufacturer Ulanqab Kema Expands Global Footprint with Advanced Functional Polymers

Ulanqab Kema’s growth is underpinned by a multifaceted strategic advantage. Its location in Ulanqab, Inner Mongolia, provides ...

MethodSense Supports ulrich medical to Fourth FDA Clearance for Innovative Computed Tomography (CT) Injector System

Collaboration underscores MethodSense’s role in accelerating market access and regulatory confidence for advanced ...

Aspire Biopharma Files Provisional Patent Application for Industry-First Sublingual Formulation of Alprazolam – Generic Xanax(R) – for Rapid Anxiety Relief

New sublingual delivery system designed to enhance bioavailability and speed of onset for major depressive and ...
WATTPoultry.com

Small US egg farms drive FDA registration growth

Discover how small US egg farms are driving FDA registrations, growing 3.5x faster than large producers and transforming the ...
QSR magazineOpinion

The FDA Just Gave You a Reprieve on Traceability. Here’s Why You Should Ignore It

As the quick-service restaurant industry digests the recent announcement that the U.S. Food and Drug Administration will ...

Aspire Biopharma Files Provisional Patent Application for Industry-First Sublingual Powder Formulation of Clopidogrel (Generic Plavix(R)) to Address Gastric Bleeding Risks

New sublingual delivery system designed to enhance bioavailability and avoid gastric side effects many patients experience with clopidogrel.
Opinion
Las Vegas SunOpinion

US drug dependence on China is a national security risk

Americans spent more than $700 billion on prescription medicines last year. However, many of them remain worried about the safety of their medications.