If you needed proof that Gordon Gekko's greed philosophy is alive and well in 2026, look no further than the pharmaceutical ...

As supply chain vulnerabilities intensify and competition accelerates, the cost of this underutilization could risk India's ...

The FDA laid out the qualifications a site would need to qualify for PreCheck on a webpage where companies can also submit ...

The legislation will impose new restrictions on pharmacy benefit managers, giant companies like CVS Caremark, Optum Rx and ...

PMMI research identifies top manufacturing hurdles including regulatory compliance, automation needs, and sustainability priorities ...

By Ahmed Aboulenein WASHINGTON, Feb 1 (Reuters) - The U.S. Food and Drug Administration on Sunday began accepting requests to ...

The FDA began accepting requests Feb. 1 to participate in its PreCheck pilot program, an initiative aimed at streamlining regulatory review for new U.S.-based pharmaceutical manufacturing facilities.

China has such a dominant position in active pharmaceutical ingredient (API) production that there is a risk it could "weaponise" access, according to a new congressional report. The document, from ...

BEND, Ore. (KTVZ) - Serán Bioscience, LLC, in collaboration with leading developer and design-builder Mortenson, hosted a topping-out ceremony on Thursday to celebrate the construction progress of a ...

On February 2, 2026, the U.S. Food and Drug Administration (FDA) published its anticipated compliance program manual, ...

Recurring stories and special news packages from C&EN. A research associate was using the company’s gas chromatography/mass spectrometry instrument to test one of the first drugs on the firm’s list: ...