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batch potency testing of immunological veterinary medicinal products
batch potency testing of immunological veterinary medicinal products
Last Update: 2011-10-23
Usage Frequency: 1
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på basis heraf skal der fremsendes en retfærdiggørelse for den minimale potency specificeret for produktet.
op grond van deze gegevens dient een rechtvaardiging geleverd te worden voor de minimum potency die gespecificeerd is voor het product.
Last Update: 2012-04-12
Usage Frequency: 2
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* relative potency (elisa test) by comparison with a reference vaccine 1
1
Last Update: 2011-10-23
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testing of residual moisture eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies
testing of residual moisture eu requirements for batches with maximum and minimum titre or batch potency for developmental safety and efficacy studies
Last Update: 2011-10-23
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så vidt muligt skal batch protokoller og specielt potency test resultater fremsendes for alle batch af h5n2 vaccine som er anvendt i det kliniske studie præsenteret i dossieret.
zo veel mogelijk batch protocollen, en met name potency testresultaten, dienen geleverd te worden voor alle batches van h5n2 vaccin die gebruikt zijn in de werkzaamheidsstudies die in het dossier geleverd zijn.
Last Update: 2012-04-12
Usage Frequency: 2
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1 flokkulations ækvivalenter; svarende til ≥ 30 ie/ ml marsvineserum i ph. eur. potency- testen
eur. potentietest
Last Update: 2011-10-23
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1 antigen enheder 2 flokkulations ækvivalenter; svarende til ≥ 30 ie/ ml marsvineserum i ph. eur. potency testen
tetanus
Last Update: 2011-10-23
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1 antigen enheder 2 flokkulations ækvivalenser; svarende til ≥ 30 ie/ ml marsvineserum i ph. eur. potency testen.
eur. potentietest
Last Update: 2011-10-23
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titel 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:
titel document 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:
Last Update: 2011-10-23
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titel på dokumentet harmonisation requirements for low and high potency and batch consistency of vaccines harmonisation requirements for low and high potency and batch consistency of vectored vaccines requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products revision: transmissible spongiform encephalopathy revision: compliance with the european pharmacopoeia revision: equine influenza revision: claims for veterinary vaccines vich:
titel document harmonisation requirements for low and high potency and batch consistency of vaccines harmonisation requirements for low and high potency and batch consistency of vectored vaccines requirements and controls applied to bovine serum used in the production of immunological veterinary medicinal products revision: transmissible spongiform encephalopathy revision: compliance with the european pharmacopoeia revision: equine influenza revision: claims for veterinary vaccines vich:
Last Update: 2011-10-23
Usage Frequency: 1
Quality:
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Please delete it you feel so.
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