American Peptide Company Announces Expansion of Its GMP Manufacturing Facility

Company expands capacity to accommodate large scale peptide production for growing customer base

29-Jan-2009 - USA

American Peptide Company, Inc. announced the expansion of its state-of-the-art GMP peptide manufacturing facility in Vista, California. The facility expansion will increase the company’s large-scale peptide production capacity as well as enable it to continue to provide high quality peptides to its growing base of pharmaceutical and biotech customers.

This two-phase expansion encompasses the construction of peptide purification and peptide synthesis suites. Four additional purification suites will be completed in the first phase and commence operation in April 2009. This addition will include new HPLC columns and tray lyophilizers.

The second phase of the construction includes two additional large-scale synthesis suites for both solution and solid phase, and completion is forecasted for Q2 in 2009. A unique component of this expansion are the 1,000 L to 2,000 L reactors for solution phase synthesis, in addition to the 260 L to 500 L SPPS for solid phase synthesis. Storage capacity will be doubled, and a 200 L tray lyophilizer will be installed to accommodate large scale production.

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HPLC is a key technology in modern analytical chemistry. It enables the separation, identification and quantification of components in complex mixtures with high precision and efficiency. Whether in the analysis of active pharmaceutical ingredients, the quality control of foodstuffs or the examination of biological samples - HPLC is often the method of choice for demanding separation tasks.

20+ products
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