Cambrex Completes First Phase of $30 Million Capacity Expansion Project in High Point, North Carolina
PR97619
EAST RUTHERFORD, NJ , Sept. 1, 2022, /PRNewswire=KYODO JBN/--
Cambrex today announced the completion of the first phase of its $30 million
investment in its small molecule active pharmaceutical ingredient (API)
manufacturing facility in High Point, North Carolina. The newly constructed
space adds analytical and chemical development laboratories totaling 30,000
square feet and provides future workspace for 85 analytical and chemical
development scientists. These laboratories will support the development of
APIs to be manufactured in the facility's current clinical manufacturing area,
as well as the future expanded clinical manufacturing and commercial
manufacturing suites.
"With the growing number of therapies in clinical development and trend toward
more targeted therapeutics, including orphan drugs, this expansion is preparing
Cambrex to support the growing demand for small-scale API manufacturing," said
Tom Loewald, CEO, Cambrex. "Our expansion goes beyond providing capacity – it
provides state-of-the-art technology and laboratory equipment, an energy
efficient infrastructure, and an ideal space for our scientific experts to work
side-by-side with our clients."
Phase 2 of the project is ongoing and will approximately double the facility's
manufacturing capacity with the addition of clinical and commercial
manufacturing suites with reactors up to 2,000 liters. The new commercial area
will provide an ideal scale for the manufacturing of orphan drugs and niche
therapies, while larger volume products developed at the facility can be
manufactured commercially at one of Cambrex's larger scale facilities in Iowa
and Sweden. This expansion follows Cambrex's 2021 investment in the Cambrex
High Point continuous flow R&D center of excellence, including expanded
capabilities for continuous flow process development, manufacturing, and scale
up.
Cambrex continues to expand its capabilities and capacity across its North
American and European network to meet the growing demand for outsourced product
development and manufacturing services.
About Cambrex
Cambrex is a leading global contract development and manufacturing organization
(CDMO) that provides drug substance, drug product, and analytical services
across the entire drug lifecycle. With over 40 years of experience and a
growing team of over 2,300 experts servicing global clients from North America
and Europe, Cambrex is a trusted partner in branded and generic markets for API
and finished dosage form development and manufacturing.
Cambrex offers a range of specialized drug substance technologies and
capabilities, including biocatalysis, continuous flow, controlled substances,
solid-state science, material characterization, stability storage, and highly
potent APIs. In addition, Cambrex can support conventional dosage forms,
including oral solids, semi-solids, and liquids, and has the expertise to
manufacture specialty dosage forms such as modified-release, fixed-dose
combination, pediatric, bi-layer tablets, stick packs, topicals, controlled
substances, sterile, and non-sterile ointments.
Contact:
Jennifer Therrien
Jennifer.therrien@cambrex.com
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SOURCE: Cambrex
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