Industry embraced prevention, but inspections, enforcement and information-sharing have struggled to keep pace. Fifteen years in, experts debate what FSMA has delivered — and what it hasn’t.

EMA and FDA have jointly issued guiding principles for the safe and responsible use of AI across the medicines life cycle, aiming to harmonize ...

WHO refuted US claims of failure and politicization, emphasizing its impartiality and historical contributions to global health. US WHO withdrawal triggers pharma regulatory and supply chain risks ...

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

Priorities include reviewing food additives, reducing diet-related chronic disease through nutrition and preventing ...

Abstract: Today, there are several monitoring tools and systems that can be used to keep the quality of drugs stored in medical environments under control. These tools are mandatory in professional ...

On December 15, 2025, the US Food and Drug Administration (FDA) issued a press release announcing that FDA eliminated a major barrier to the use ...

The "GMP Auditing for Quality Assurance Training Course for FDA Regulated Industries (Jan 28th - Jan 29th, 2026)" training has been added to ResearchAndMarkets.com's offering.

Automation in 2026 is no longer judged by the volume of experiments, but by the reliability of the evidence they produce. As complex biology and tighter budgets collide, industry leaders are pivoting ...

This site displays a prototype of a “Web 2.0” version of the daily Federal Register. It is not an official legal edition of the Federal Register, and does not replace the official print version or the ...

The majority of primary care physicians report that drug shortages affect the quality of patient care and increase administrative burdens, according to new research published in JAMA Network Open. The ...