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Manufacturing News

FDA Opens PreCheck Program for Domestic Manufacturing

The FDA officially launched its Manufacturing PreCheck Pilot Program on February 1, 2026, introducing a two-phase regulatory framework designed to accelerate construction and approval of new U.S. pharmaceutical manufacturing facilities. The initiative arrives as the contract development and manufacturing organization

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CDMO News

WuXi Vaccines Achieves ANVISA GMP Approval for DP17 Site in Suzhou

WuXi Vaccines, a vaccine-focused CDMO and wholly owned subsidiary of WuXi Biologics, has received Good Manufacturing Practices (GMP) certification from Agência Nacional de Vigilância Sanitária (ANVISA) for its DP17 fill and finish facility in Suzhou. The certification follows comprehensive on-site

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