[引用][C] PDA Technical Report No. 41: Virus Filtration
G Sofer, K Brorson, A Abujoub, H Aranha… - PDA Journal of …, 2005 - hub.tmu.edu.tw
PDA Technical Report No. 41: Virus filtration — 臺北醫學大學 跳至主導覽 跳至搜尋 跳過主要
內容 臺北醫學大學 首頁 臺北醫學大學 Logo 說明與常見問題 English 中文 首頁 專家檔案 研究 …
內容 臺北醫學大學 首頁 臺北醫學大學 Logo 說明與常見問題 English 中文 首頁 專家檔案 研究 …
Removal of virus through novel membrane filtration method.
S Manabe - Developments in biological standardization, 1996 - europepmc.org
To protect against virus infections, the new technology of the virus removal membrane has
been developed. The novel virus removal filter PLANOVA is validated for virus removal, that …
been developed. The novel virus removal filter PLANOVA is validated for virus removal, that …
[HTML][HTML] Virus removal by filtration: points to consider
G Kern, M Krishnan - BioPharm International, 2006 - biopharminternational.com
Virus safety of biotech-and plasma-derived therapeutics is ensured through complementary
manufacturing and quality control measures that include the control and monitoring of raw …
manufacturing and quality control measures that include the control and monitoring of raw …
[引用][C] Single‐use virus clearance technologies in biopharmaceutical manufacturing: case studies
S Ray, S Dolan - Single‐Use Technology in Biopharmaceutical …, 2010 - Wiley Online Library
Single-Use Virus Clearance Technologies in Biopharmaceutical Manufacturing: Case
Studies Page 1 Single-Use Virus Clearance Technologies in Biopharmaceutical …
Studies Page 1 Single-Use Virus Clearance Technologies in Biopharmaceutical …
Proceedings of the 2011 Viral Clearance Symposium (South San Francisco, CA)
K Brorson, R Levy - PDA Journal of Pharmaceutical Science and …, 2014 - journal.pda.org
Freedom from viral contaminants is a paramount concern for recombinant
biopharmaceuticals and plasma-derived medicinal products. Viral safety is achieved by a …
biopharmaceuticals and plasma-derived medicinal products. Viral safety is achieved by a …
Viral clearance of traditional unit operations: virus-retentive filtration
Q Chen, D Chen - PDA Journal of Pharmaceutical Science and …, 2015 - journal.pda.org
Retentive filters designed to provide effective and consistent clearance of parvovirus (∼ 20
nm) have now become a standard in downstream purification processes for biologics …
nm) have now become a standard in downstream purification processes for biologics …
Advances in viral clearance
K Brorson - Process scale bioseparations for the …, 2006 - taylorfrancis.com
The viral safety of biotechnology products has traditionally been a key concern both of
regulators and industry. 1-6 It has also proven to be a stumbling block for early product …
regulators and industry. 1-6 It has also proven to be a stumbling block for early product …
Proceedings of the 2009 Viral Clearance Symposium.
G Miesegaes, M Bailey, H Willkommen… - Developments in …, 2010 - europepmc.org
The 2009 Viral Clearance Symposium (Indianapolis, IN, USA) was held to interactively
discuss methods for virus removal and inactivation during biopharmaceutical manufacture …
discuss methods for virus removal and inactivation during biopharmaceutical manufacture …
Investigations into the Fouling mechanism of parvovirus filters during filtration of freeze–thawed mAb drug substance solutions
JG Barnard, D Kahn, D Cetlin, TW Randolph… - Journal of …, 2014 - Elsevier
Filtration to remove viruses is one of the single most expensive steps in the production of
mAb drug products. Therefore, virus filtration steps should be fully optimized, and any …
mAb drug products. Therefore, virus filtration steps should be fully optimized, and any …
Impact of proteins and protein fouling on virus retention during virus removal filtration
Virus filtration is a crucial step in ensuring the high levels of viral clearance required in the
production of biotherapeutics produced in mammalian cells or derived from human plasma …
production of biotherapeutics produced in mammalian cells or derived from human plasma …