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Separation Systems for Commercial Biotechnology
Date:9/21/2011

ical development. Protein separation systems do not require U.S. Food and Drug Administration (FDA) approval, but the products produced from these processes do, and they must be produced in accordance with FDA good manufacturing practices (GMP) guidelines. Thus, these separation procedures and equipment must pass FDA audits of the manufacturing process. New products requiring separation technologies that have been approved by the FDA in 2009 and 2010 are covered, and those products expected to be approved within the forecast period are discussed. Due to the timing of the writing of this report, the figures for 2011 are estimated except where actual results have been reported

The report includes analysis of the leading competitors, as well as emerging companies in the current global biomolecule separation market. Profiles of the manufacturers of the leading products are analyzed, and their specific product strategies are outlined. This report notes companies that are poised to introduce new products during the forecast period and discusses how these products may change the face of the competitive environment. This competitive environment is examined, with a special focus on the ways in which developing products and technologies are influencing the current standard of patient care. Detailed profiles of the current market leaders and emerging companies are discussed in detail.

Market figures are based on revenues at the manufacturers' level. The base year for analysis and projection is 2010. Trends are assessed based on a number of parameters, including projected sales for existing products, new product INTRODUCTIONs, and expanded indications for existing products.

This report also includes overviews and forecasts of the separations market by product, by company, and by geographic region for the period from 2010 to 2016. The global market is analyzed, and data are provided for each segment.

Sales figures are reported in U.S. dollars
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