The 2000 study in the scientific journal Regulatory Toxicology and Pharmacology had concluded that the active ingredient in ...

The decision of Elsevier, a Dutch academic publishing company, to retract a safety evaluation and risk assessment of the herbicide Roundup and its active ingredient, glyphosate, for humans, is causing ...

Oil spill impact assessment has evolved from physics-based trajectory modeling toward multidisciplinary frameworks that ...

Q4 2025 Earnings Call Transcript December 4, 2025 Operator: Hello, and welcome, everyone joining today’s Inotiv Fourth ...

Per- and polyfluoroalkyl substances (PFAS), often referred to as “forever chemicals,” are a very diverse set of organic chemical compounds ...

On , The US Food and Drug Administration issued draft guidance identifying specific types of monoclonal antibody products for which the agency believes six-month toxicity testing in non-human primates ...

A University of Cambridge study has identified 168 everyday chemicals that are toxic to beneficial gut bacteria and can ...

A paper purportedly demonstrating the safety of glyphosate that has historically been “a cornerstone in the assessment of ...

US FDA releases draft guidance on reducing testing on non-human primates for monoclonal antibodies: Silver Spring, Maryland Thursday, December 4, 2025, 09:00 Hrs [IST] The US Food ...

The draft guidance issued Tuesday comes as regulators and policymakers have looked for ways to aid U.S. drugmakers amid fast progress by their China-based counterparts.

While welcomed by the pros, volunteers fear disbanding the ACC panel will make it more difficult to access help.

The retraction of the glyphosate safety report comes as the Trump admin throws support behind Roundup lawsuit appeal.