HANGZHOU CITY, ZHEJIANG, CHINA, January 19, 2026 /EINPresswire.com/ -- With the development of the pharmaceutical and ...

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 ...

XINTAI, SHANDONG, CHINA, January 19, 2026 /EINPresswire.com/ -- In recent years, the global pharmaceutical packaging ...

Laine Mello, director of Marketing at Ecolab for its bioprocessing business, shares her insights on the digital ...

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

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.

On February 1, FDA announced a new pilot program designed to promote the construction of domestic manufacturing sites, along ...

The PreCheck programme, first unveiled in June 2025, aims to speed up drug facility construction.

In today’s Pharmaceutical Executive Daily, tariff uncertainty triggers a short-term surge in pharmaceutical manufacturing ...

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

While braille is mandatory on all pharmaceutical packaging in Europe, U.S. regulatory agencies remain quiet on the issue, according to Pharmaceutical Processing. The U.S. Food and Drug Administration ...

Gov. Josh Shapiro and Pennsylvania Department of Community & Economic Development (DCED) Secretary Rick Siger this week announced the Commonwealth has secured a $3.5 billion private-sector investment ...