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Journal Abstract Search

227 related items for PubMed ID: 9413685

  • 1. In-process testing and limits.
    Sjöholm I.
    Dev Biol Stand; 1997; 91():73-8. PubMed ID: 9413685
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  • 5. Raw material considerations.
    Lubiniecki AS, Shadle PJ.
    Dev Biol Stand; 1997; 91():65-72. PubMed ID: 9413684
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  • 6. FDA perspective on specifications for biotechnology products--from IND to PLA.
    Murano G.
    Dev Biol Stand; 1997; 91():3-13. PubMed ID: 9413677
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  • 8. The use of bioassays for the characterisation and control of biological therapeutic products produced by biotechnology.
    Thorpe R, Wadhwa M, Mire-Sluis A.
    Dev Biol Stand; 1997; 91():79-88. PubMed ID: 9413686
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  • 9. The role of assay validation in specification development.
    Baffi RA.
    Dev Biol Stand; 1997; 91():105-13. PubMed ID: 9413687
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  • 11. Global regulatory considerations for unified assay specifications.
    Patterson S, Lin L, Elchico J, Fuchs R, Powell S, Redhair D, Warwick M, Solli N, Méndez B.
    Dev Biol Stand; 1997; 91():45-8. PubMed ID: 9413682
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  • 13. Biosimilars and biopharmaceuticals: what the nephrologists need to know--a position paper by the ERA-EDTA Council.
    Covic A, Cannata-Andia J, Cancarini G, Coppo R, Frazão JM, Goldsmith D, Ronco P, Spasovski GB, Stenvinkel P, Utas C, Wiecek A, Zoccali C, London G.
    Nephrol Dial Transplant; 2008 Dec; 23(12):3731-7. PubMed ID: 18802209
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  • 14. Quality-by-design for biotechnology-related pharmaceuticals.
    Mandenius CF, Graumann K, Schultz TW, Premstaller A, Olsson IM, Petiot E, Clemens C, Welin M.
    Biotechnol J; 2009 May; 4(5):600-9. PubMed ID: 19418475
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