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points to consider on quality aspects of medicinal products containing active substances produced by stable transgene experession in higher plants
points to consider on quality aspects of medicinal products containing active substances produced by stable transgene experession in higher plants
european drug master file declaration of storage conditions for pharmaceutical veterinary medicinal products in the product particulars and active substances:
european drug master file declaration of storage conditions for pharmaceutical veterinary medicinal products in the product particulars and active substances:
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
titel på dokumentet note for guidance on the use of bovine serum in the manufacture of human biological medicinal products points to consider on quality aspects of medicinal products containing active substances produced by stable transgene expression in higher plants revision of note for guidance on minimising the risks of tse transmission via medicinal products points to consider on the development of live attenuated influenza vaccines
título del documento note for guidance on the use of bovine serum in the manufacture of human biological medicinal products points to consider on quality aspects of medicinal products containing active substances produced by stable transgene expression in higher plants revision of note for guidance on minimising the risks of tse transmission via medicinal products points to consider on the development of live attenuated influenza vaccines
stability testing of existing active substances and related finished products summary of requirements for active substances process validation (update) quality aspects of veterinary medicinal products administered via drinking water
stability testing of existing active substances and related finished products summary of requirements for active substances process validation (update) quality aspects of veterinary medicinal products administered via drinking water
den fuldstændige risikovurderingsrapport og et resumé af den ligger på det europæiske kemikaliekontors internetsted, http://ecb.jrc.it/existing-substances/
el informe completo de evaluación del riesgo, así como un resumen del mismo, pueden consultarse en la página internet de la oficina europea de sustancias químicas: http://ecb.jrc.it/existing-substances/
alle logitech produkter overholder eu's rohs-direktiv (european directive on the restriction of the use of certain hazardous substances in electrical and electronic equipment).
todos los productos logitech cumplen las estipulaciones de la directiva rohs de la ue sobre restricciones de sustancias peligrosas (relativa a la utilización de determinadas sustancias peligrosas en aparatos eléctricos y electrónicos).