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journal of immunological methods, 93, 115-121.11.
journal of immunological methods, 93, 115 to 121.11.
最后更新： 2014-11-21
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batch potency testing of immunological veterinary medicinal products
batch potency testing of immunological veterinary medicinal products
最后更新： 2011-10-23
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reduce the time to reach clinical proof of concept in immunological, respiratory, neurological and neurodegenerative diseases
reduce the time to reach clinical proof of concept in immunological, respiratory, neurological and neurodegenerative diseases;
最后更新： 2017-04-06
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in- use stability testing of veterinary medicinal products (excluding immunological veterinary medicinal products)
in-use stability testing of veterinary medicinal products (excluding immunological veterinary medicinal products)
最后更新： 2011-10-23
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requirements and controls applied to bovine serum (foetal or calf) used in the protection of immunological veterinary medicinal products
requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products
最后更新： 2011-10-23
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i. development and method of elisa.« journal of immunological methods, 93, 115-121.11.
i. development and method of elisa.’ journal of immunological methods, 93, 115 to 121.11.
最后更新： 2014-11-12
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field trials with veterinary vaccines requirements and controls applied to bovine serum (foetal or calf) used in the protection of immunological veterinary medicinal products
requirements and controls applied to bovine serum (foetal or calf) used in the protection of immunological veterinary medicinal products released for consultation october 2000
最后更新： 2011-10-23
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cvmp-arbejdsgruppe vedrørende immunologiske veterinærlægemidlertitel på dokumentet requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies requirements for live recombinant vectored vaccines requirements for compatibility statements for veterinary vaccines harmonisation of requirements for potency and batch consistency of vaccines vich:
cvmp immunologicals working party document title requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies requirements for live recombinant vectored vaccines requirements for compatibility statements for veterinary vaccines harmonisation of requirements for potency and batch consistency of vaccines vich:
最后更新： 2008-03-04
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