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The new suites include full serialization capabilities, specifically designed for small-scale batches of commercial products. Validation of the equipment is expected to be completed by the end of Q1 2022.

“Advanced therapeutics require increasingly complex handling requirements, and the investment we have made in Philadelphia allows Catalent to operate efficient packaging processes and operations, bridging the gap between clinical scale and niche commercial volumes,” commented Ann McMahon, General Manager of Commercial & Integrated Development Operations at Catalent Clinical Supply Services. “The specifically designed packaging areas not only provide optimal commercial opportunities for drug developers, but also the safest working conditions for employees in terms of air exchange rates, carbon dioxide monitoring, and ultraviolet air sanitization.”

The 200,000 square-foot Philadelphia facility is the largest site in Catalent’s global clinical supply network and the company’s North American Center of Excellence for clinical supply packaging. It includes an on-site pharmacy to support FlexDirect® direct-to-patient services for clinical trials, as well as access to Catalent’s FastChain® demand-led supply services, primary and secondary packaging capabilities, a range of temperature options for storage and distribution, and clinical returns and destruction services.

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