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34 Results Found

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  1. Hepatitis E virus derived from different sources exhibits different behaviour in virus inactivation and/or removal studies with plasma derivatives

    Author
    Yunoki, M., et al
    Organization
    Japan Blood Products Organization
    Publisher
    Biologicals 44(5) 403-411
    Year
    2016
    Access
    Abstract Only
  2. Pathogen safety of a pasteurized four‐factor human prothrombin complex concentrate preparation using serial 20N virus filtration

    Author
    Nowak, T., et al
    Organization
    CSL Behring
    Publisher
    Transfusion 57(5) 1184-1191
    Year
    2017
    Access
    Open
  3. Pathogen Safety of a New Intravenous Immune Globulin 10% Liquid

    Author
    Radomski, K., et al
    Organization
    Octapharma Biopharmaceuticals GmbH
    Publisher
    BioDrugs (2017) 31: 125
    Year
    2017
    Access
    Open
  4. Evaluation of the virus clearance capacity and robustness of the manufacturing process for the recombinant factor VIII protein, turoctocog alfa

    Author
    Ellgaard, T., et al
    Organization
    Novo Nordisk A/S
    Publisher
    Protein Expression and Purification 129 (2017) 94-100
    Year
    2017
    Access
    Open
  5. Validation of the manufacturing process used to produce long-acting recombinant factor IX Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Haemophilia 20(4): e327-e335
    Year
    2014
    Access
    Open
  6. BAY 81-8973, a full-length recombinant factor VIII: manufacturing processes and product characteristics

    Author
    Garger, S., et al
    Organization
    Bayer
    Publisher
    Haemophilia 23(2): e67-e78
    Year
    2017
    Access
    Open
  7. Manufacturing process used to produce long-acting recombinant factor VIII Fc fusion protein

    Author
    McCue, J., et al
    Organization
    Biogen
    Publisher
    Biologicals 43: 213–219
    Year
    2015
    Access
    Open
  8. Pathogen safety and characterisation of a highly purified human alpha1-proteinase inhibitor preparation

    Author
    Kee, S., et al
    Organization
    CSL Behring
    Publisher
    Biologicals 47: 25–32
    Year
    2017
    Access
    Open
  9. Validation and implementation of Planova™ BioEX virus filters in the manufacture of a new liquid intravenous immunoglobulin in China"

    Author
    Ma, S., et al.
    Organization
    Shandong Taibang Biological Products Co., Ltd. and Asahi Kasei Medical Co., Ltd.
    Publisher
    Biologicals 52 (2018) 37-43
    Year
    2018
    Access
    Abstract Only
  10. Characterizing the Impact of Pressure on Virus Filtration Processes and Establishing Design Spaces to Ensure Effective Parvovirus Removal

    Author
    Strauss, D., et al
    Organization
    Asahi Kasei Bioprocess America
    Publisher
    Biotechnology Process e-pub
    Year
    2017
    Access
    Open