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harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain
h a r m o n is a t ion of requirements for e q u ine influe n z a v a c c ine s s p e c ific r e q u ir e m e n t s f o r s u b s t itutio n o r

hoap— harmonisation of overseas audit practice (harmonização das práticas de auditoria no ultramar)
hoap— "harmonisation of overseas audit practice" (armonización de prácticas de fiscalización en el extranjero)

estimation of predicted environmental concentrations, including harmonisation of default values and development of a harmonised computer model toxicity of substances to dung fauna degradation of substances in manure
pre-approval information for registration of new medicinal products for food producing animals with respect to antimicrobial resistance injection site residues user safety estimation of predicted environmental concentrations, including harmonisation of default values and development of a harmonised computer model toxicity of substances to dung fauna degradation of substances in manure

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 .

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

título 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)

concept paper on the revision of the cpmp/ bwp note for guidance (cpmp/ bwp/ 214/ 96) on harmonisation of requirements for influenza vaccines
concept paper on the revision of the cpmp/bwp note for guidance (cpmp/bwp/214/96) on harmonisation of requirements for influenza vaccines