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harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain
según se anticipaba en el programa de trabajo para 1998-99, este paso positivo ha contribuido ya a aumentar el número de solicitudes centralizadas en el sector veterinario.

vuonna 1992 eurostat ja työllisyyden ja sosiaaliasioiden pääosasto julkaisivat teoksen "methodology for the harmonisation of european occupational
eurostat y la dg empleo y asuntos sociales publicaron en 1992 la «metodología para la armonización de las estadísticas europeas de accidentes de trabajo» (11).

this enhanced community involvement will also increase harmonisation of national approaches and tap into potential synergies by including experts from other member states in in-depth monitoring visits .
this enhanced community involvement will also increase harmonisation of national approaches and tap into potential synergies by including experts from other member states in in-depth monitoring visits .

approach towards harmonisation of withdrawal periods ” (emea/ cvmp/ 036/ 95- final) mukaisesti.
approach towards harmonisation of withdrawal periods” (emea/ cvmp/ 036/ 95-final).

note for guidance on cell culture inactivated influenza vaccines – annex to note for guidance on harmonisation of requirements for influenza vaccines cpmp/ bwp/ 214/ 96
note for guidance on cell culture inactivated influenza vaccines – annex to note for guidance on harmonisation of requirements for influenza vaccines cpmp/ bwp/214/96

asiakirjan nimi 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:
título del documento 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:

note for guidance on cell culture inactivated influenza vaccines annex to nfg on harmonisation of requirements for influenza vaccines (cpmp/ bwp/ 214/ 96)
número de referencia título del documento cpmp/ bwp/ 2490/ 00 note for guidance on cell culture inactivated influenza vaccines annex to nfg on harmonisation of requirements for influenza vaccines (cpmp/ bwp/ 214/ 96)

asiakirjan nimi 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:
título del documento 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: