Catalent Plans To Increase Biologic Development And Manufacturing Capabilities

Catalent Announces Plans to Increase Biologic Development and Manufacturing Capabilities

Somerset, NJ, December 7, 2011 — Catalent Pharma Solutions, a leading provider of drug and biologic development services, delivery technologies and supply solutions, announces plans to expand its biologics facility by relocating to a new facility in Madison, Wisconsin in late 2012 to provide increased capacity for seamless cell line and biomanufacturing solutions for innovators to speed time to clinic. Catalent’s current facility is located in Middleton, Wisconsin.

The new facility will quadruple the capacity of Catalent’s current facility, allowing the company to enhance its offerings in the development and manufacturing of biologic products.  Additionally, the expansion will enhance the efficiency and output of Catalent’s GPExâ cell line engineering technology and process development capabilities, as well as other mammalian cell lines.  This combination of technology and capabilities is designed to provide Catalent’s customers with a competitive advantage by producing stable, high-yielding mammalian cell lines and robust manufacturing processes with industry leading timelines.  

“Plans for the biologics facility are designed to meet our customers’ needs through improved delivery of integrated services in the areas of biologic development and manufacturing,” stated Kent Payne, Ph.D., Vice President and General Manager of Catalent’s Biologics business. “This is the first step in a series of strategic development initiatives designed to enhance our offerings in this rapidly expanding market.”

Supported by numerous process upgrades and increased capabilities in process development, the new facility will include three individual current Good Manufacturing Practice (cGMP) compliant production suites that will increase Phase I and II production capacity up to 1,000L bioreactors.

Catalent will also transition from stainless steel bioreactors to single use bioreactors.  This transition will further increase capacity by increasing the number of batches produced per suite and allow greater flexibility in the scale of cGMP manufacturing capacity offered to Catalent’s customers.

About Catalent

From drug and biologic development services to delivery technologies to supply solutions, Catalent Pharma Solutions has the deepest expertise, the broadest offerings and the most unique technologies in the industry. With over 75 years of experience, Catalent helps customers get more molecules to market faster, enhance product performance, and provide superior, reliable manufacturing and packaging solutions. Catalent employs more than 8,000 people at 20+ facilities worldwide and in fiscal year 2011 generated more than $1.6 billion in annual revenue. Catalent is headquartered in Somerset, NJ.

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