Recent site upgrades, acquisitions, and new partnerships demonstrate a shift from cost-driven outsourcing to integrated, locally anchored models, says the firm.
The company’s expansion adds 70,000 square feet to the facility and two isolated filling lines for syringes, cartridges, and vials, as well as lyophilization and packaging capabilities.
The CDMO’s Texas facility has supported six client programs expected to reach Investigational New Drug submission this year, following its 100th GMP batch in July.
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