Results for process requirements for inform... translation from Danish to Portuguese

læs indlægssedlen for information.
ver o folheto informativo para mais informações.

specific requirements for canines
specific requirements for canines

det europæiske samarbejdsområde for information
o espaço Único europeu da informação

requirements for combined veterinary vaccines
requirements for combined veterinary vaccines

talsmandens gruppe og generaldirektoratet for information
informação, comunicação e cultura

omstrukturering af universitetsledelsessystemer, infrastruktur for information
desenvolvimento de estudos europeus

direktorat d - fri bevægelighed for information.
direcção d — livre circulação da informação.

requirements for compatibility statements for veterinary vaccines
requirements for compatibility statements for veterinary vaccines

- de særlige behov for information ved selvmedicinering
- às necessidades específicas de informações relativas à automedicação,

efficacy on anthelmintics: specific requirements for canine
efficacy on anthelmintics: specific requirements for canine

suppleant@ item non- participant copied for information
participante opcional@ item non- participant copied for information

europÆiske fÆllesskaber generaldirektoratet for information, kommunikation, kultur
direcção­geral informação, comunicação, cultura

requirements for pharmaceutical documentation for pressurised metered dose inhalation products
ich q1f stability data package for registration in climatic zones iii and iv requirements for pharmaceutical documentation for pressurised metered dose inhalation products

note for guidance on requirements for pharmaceutical documentation for pressurised metered dose inhalation products
note for guidance on requirements for pharmaceutical documentation for pressurised metered dose inhalation products

harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain
harmonisation of requirements for equine influenza vaccines specific requirements for substitution or addition of a strain

concept paper on the development of a cpmp note for guidance on requirements for the evaluation of new adjuvants in vaccines
note for guidance on the use of bovine serum in the manufacture of human biological medicinal products concept paper on the development of a cpmp note for guidance on requirements for the evaluation of new adjuvants in vaccines

tak for informationen.
obrigado pela informação.

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

brugerne bør have tillid, så de på frivillig basis bidrager til processen med at skabe et sikrere samfund for information.
os utilizadores deverão ter confiança na segurança da sociedade da informação e sentir ­ se protegidos do crime e de violações da sua privacidade.

position paper on the regulatory requirements for the authorisation of low- dose modified release asa formulations in the secondary prevention of cardiovascular events.
position paper on the regulatory requirements for the authorisation of low- dose modified release asa formulations in the secondary prevention of cardiovascular events.