Virus Filtration Market Share, Size, Growth & Forecast 2024 Illuminated by New Report Date: 03-01-2017 12:10 AM CET Category: Health & Medicine Press release from: Transparency Market Research - Pharmaceutical
Virus filtration is an important procedure in the pharmaceutical industry. It ensures the purity and steady consumption of valuable products, besides optimizing the economic process and preventing loss. Virus filtration feed streams generally exhibit high purity and heavy product concentrations. Retrovirus and parvovirus filtration membranes are two ultrafiltration membranes tested (and their performances compared) using realistic model feed streams consisting of minute virus of mice (recommended from FDA). This approach provides an industry-relevant benchmark for the engineering competence of virus filters. Asymmetric membranes operate in direct flow and in a constant pressure mode in accordance with the industrial practice of virus filtration. However, new developments in research and development using flux method allow to image at the performance of virus filtration and similar ultrafiltration membranes, which also provides insights into designing virus filtration membranes. Browse Global Strategic Business Report: www.transparencymarketresearch.com/virus-filtration-marke... Hike in R&D expenditure, development of the biopharmaceutical industry, and increasing government funding for the biotechnology and pharmaceutical industries are driving the global virus filtration market. According to the parenteral drug association, parvovirus filters in the downstream process have become an industry standard and a common regulatory expectation in the recent years. The filters consistently demonstrate highly effective retrovirus retention without impacting the quality of the product across a wide range of parameters and are an effective method to reduce virus risks in biopharmaceutical manufacturing. The filtration technique needs to be approved by the U.S. food and drug administration (FDA). Regulatory agencies in Germany and France require the manufacturing processes to be evaluated and the units to be cleared of the multiple models of relevant viruses before being marketed as authorization. These stringent government validation practices are expected to be a hindrance for the global virus filtration market. The market has been segmented by product type, application, end-users, and geography. In terms of product type, it is classified into the following categories: virus filters, kits and reagents, filtration systems, and others. It majorly has biological
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