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Dunhua 2

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Asymchem’s dedicated carbapenem facility completes first United States FDA inspection

Pharma & Biotech

Why Asymchem’s first FDA inspection at Dunhua 2 matters far beyond one carbapenem API

by Pallavi Madhiraju
July 25, 2026
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Asymchem’s Dunhua 2 site completes its first FDA inspection, advancing continuous carbapenem API manufacturing and U.S. supply readiness.

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Representative image of biopharma laboratory research. Gilead Sciences and Merck’s latest Phase 3 updates highlight the promise of once-weekly HIV treatment with islatravir and lenacapavir, while raising fresh questions over Trodelvy’s lung cancer expansion strategy.

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clinical trials Eli Lilly and Company European Medicines Agency FDA FDA approval immuno-oncology immunotherapy Inc. Johnson & Johnson medical devices oncology precision oncology rare disease U.S. Food and Drug Administration United States Food and Drug Administration

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