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Dowpharma Sharpens Focus on New Expression Systems; Smithfield Facility Will be Closed Smithfield, RI - July 29, 2004 Dowpharma, a business unit of The Dow Chemical Company, has announced plans to close its biopharmaceutical contract manufacturing facility in Smithfield, Rhode Island. Dowpharma will continue to develop its biopharmaceutical contract manufacturing business by building on promising new developments in protein and peptide expression technologies that will contribute significantly to the pharmaceutical industry's drive for accessible, affordable medicines. To enable this, Dow previously announced the consolidation of its process development capability at Dow's biotechnology center in San Diego and recently launched its Pseudomonas fluorescens expression technology for the production of recombinant proteins. This novel technology can increase cellular expression while maintaining critical solubility and activity characteristics of recombinant proteins. Also this year, Dowpharma announced a new peptides offering, including expression and purification strategies for cost effective manufacturing. Dowpharma will also focus on plant-based systems, having made several recent announcements about its expanded offerings to the industry in antibody expression and peptide expression. "These offerings allow both rapid scale up and higher productivity for complex proteins," Hyde added. "Dowpharma is committed to offering tailored solutions to our clients through our expanding technical portfolio and key partnerships with other companies. We will continue to invest in opportunities to become a long-term leader in biopharmaceutical manufacturing by using our science base and operational expertise to help bring affordable medicines to market faster," stated Hyde. About Dowpharma Dowpharma services include process development, route selection, methods development, custom solubilization, including BioAqueous* solubilization services, chiral capabilities, and associated analytical services, biotargeted radiopharmaceuticals development through ChelaMed* radiopharmaceutical services, as well as manufacturing and scale-up from feasibility, through clinical trials, to commercial manufacturing. Dowpharma currently manufactures small molecule Active Pharmaceutical Ingredients (APIs) and intermediates, oligonucleotides, cGMP polymers, peptides and therapeutic proteins from microbial fermentation, including a novel Pseudomonas fluorescens-based expression technology, and plant-based systems. Dowpharma draws upon over 30 years of excellent cGMP regulatory compliance in the organic synthesis of APIs and pharmaceutical intermediates with the ability to provide client support in filing and validation strategies. Dowpharma operates research, process development, and manufacturing facilities in North America and Europe. More information is available at www.dowpharma.com. About Dow For Editorial Information: Kathleen Davis |
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