
PTSM: Pharmaceutical Technology Sourcing and Management
- PTSM: Pharmaceutical Technology Sourcing and Management-10-07-2015
- Volume 11
- Issue 10
Hovione Expands Drug Substance Manufacturing
Hovione will double its manufacturing capacity in New Jersey with an expanded facility and a commercial spray dryer designed to handle potent APIs.
Hovione is expanding its facility in New Jersey as part of the company’s strategy to increase its global development and commercial capacity, the company announced on Sept. 29, 2015. The expansion will add an additional 30,600 ft² (2843 m²) to the 24,000 ft² (2,211m²) facility. It will introduce a new commercial spray dryer unit to complement an existing pilot unit, and this installation will be specifically designed to handle potent drug substances (APIs). With this new equipment, Hovione will offer commercial-scale spray drying in Portugal, Ireland, and the US. In addition, the expansion will more than double the drug substance capacity at the site to support the needs of the current and future customer base.
“Expanding our manufacturing presence in the US highlights our commitment to our customers that want to manufacture their products in the US and to support the development needs of our ever expanding local customer base. The additional capacity will give us more flexibility and make us more agile to deal with our customer’s fast paced projects,” said Marco Gil, general manager, Hovione New Jersey, in a press release.
The official ground breaking should occur in the first quarter of 2016 and the doubling of capacity is expected to be fully operational in early 2017. The expansion is expected to add approximately 60 new jobs to the current workforce.
Source:
Articles in this issue
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FDA Plans Pilot Projects for Drug Supply Chain Security Actabout 10 years ago
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Tecnandina’s Ecuador Facility Receives ANVISA Certificationabout 10 years ago
Piramal Introduces Proof of Concept Service for Next Wave of ADC Growthabout 10 years ago
Patheon Unveils New Brand Identityabout 10 years ago
FDA Releases Guidance on Generic-Drug Developmentabout 10 years ago
Kopcha Selected to Head FDA’s Quality OfficeNewsletter
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