Bora Pharmaceuticals Announces Multi-Year Expansion for Midwest Manufacturing Site, as Upsher-Smith Entity Split is Finalized
Buildout includes Gerteis Macro-Pactor® install, with additional investments to follow, to meet industry demand at
As the entity separation from
“With pharmaceutical companies relying more heavily on specialized CDMO partners to scale production and maintain quality, top-tier manufacturing capacity and technical expertise are at a premium,” said J.D. Mowery, president of Bora’s CDMO business. “Bora’s
The first phase of Bora’s investment will add a Gerteis Macro-Pactor® at the company’s state-of-the-art site. This investment initiates a broader buildout of 100,000 square feet of dedicated shell space designed to streamline production for partners with high-volume needs.
The Gerteis Macro-Pactor® roller compactor will be installed and operational in the third quarter of 2025.
“As we complete our transition from
The facility offers on-site quality control laboratories and a dedicated development team to support product and analytical development as well as innovation. It is an FDA-inspected manufacturing site and meets global health authority requirements, ensuring regulatory compliance.
From early development and scale-up to process optimization and commercial manufacturing, Bora’s experienced teams support customers at every stage of the product lifecycle. The company’s commercial on-time, in-full (OTIF) delivery record is unmatched, reinforcing Bora’s role as a trusted partner, supporting clients with secure, consistent supply. For more information, visit boracdmo.com
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