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guideline for the photostability testing of new drug substances and products
guidelines for the photostability testing of new drug substances and products
note for guidance on impurities testing: impurities in new drug substances
note for guidance on impurities testing: impurities in new drug substances
ich q1d – bracketing and matrixing designs of drug substances and drug products
ich q1d – bracketing and matrixing designs of drug substances and drug products
guidelines assessment of the effect of antimicrobial substances on dairy starter cultures
assessment of the effect of antimicrobial substances on dairy starter cultures
note for guidance on stability testing of new drug substances and products step 2 document
note for guidance on stability testing of new drug substances and products step 2 document
good clinical practices stability testing of existing active substances and related finished products
via duca di calabria, 1/1 casella postale 552 i-50125 firenze
annex to note for guidance on stability testing of new active substances and medicinal products.
annex to note for guidance on stability testing of new active substances and medicinal products.
annex to note for guidance on stability testing of existing active substances and related finished products.
annex to note for guidance on stability testing of existing active substances and related finished products.
titel på dokumentet safety evaluation of antimicrobial substances regarding the effects on human gut flora vich:
título del documento safety evaluation of antimicrobial substances regarding the effects on human gut flora vich:
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:
mepc.2/circular, provisional categorization of liquid substances, version 14, gældende fra 1. januar 2009.
mepc. 2/circular, categorización provisional de sustancias líquidas, versión 14, con efecto desde el 1 de enero de 2009.
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).