Cambrex Acquires Biopharmaceutical Producer
The 65,000 square foot facility contains two fully validated suites dedicated to various biologic processes and adequate space for three additional cGMP suites. The US FDA has successfully inspected the existing suites. Current production capabilities include bacterial and yeast fermentation units up to a capacity of 800 liters, small and large-scale purification, and a 1500+ vial filling facility for Phase I and Phase II clinical trials. Full year 2001 sales revenues are targeted at approximately $8.5 million. Sales revenues in 2002 are expected to grow in excess of 50%.
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