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Viral Clearance Market will worth USD 510.3 Million in 2020
Download PDF Brochure @ http://tinyurl.com/Viral-Clearance-PDF Viral clearance study is carried out by manufacturers to detect virus contaminations in biologics and other products. Viral clearance testing is necessary by regulatory authorities for investigational new drug (IND) submission and is mainly critical in process development for biologicals including tissue and tissue products, stem cell products, cellular and gene therapy products, blood and blood products, and vaccine and therapeutics. Viral clearance studies helps to analyze the effectiveness of each step in manufacturing process to remove or inactivate potential contaminant viruses. The global viral clearance market was valued at USD 285.5 Million in 2015 and poised to grow at a CAGR of 12.3% between 2015 and 2020, to reach USD 510.3 Million in 2020. In this report, the global viral clearance market is segmented based on method, end user, application, and geography. The method segments included in the report are viral detection method, viral removal method, and viral inactivation method. The viral detection method is further subsegmented into plaque assays, PCR, ELISA, and other viral detection method. Other viral detection method includes western blot, transmission EM, in vivo assay, in vitro assay, and NGS (Next Generation Sequencing). The viral removal method is further subsegmented in to chromatography, nanofiltration, and precipitation. The viral inactivation method is further subsegmented in to solvent detergent method, pasteurization, and other viral inactivation method. Other viral inactivation method includes low pH, microwave heating, irradiation, and high-energy light.
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