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  • European Medicines Agency (EMA)
    The European Medicines Agency is a decentralised agency of the European Union responsible for the evaluation, supervision and safety monitoring of medicines
  • Medicines | European Medicines Agency (EMA)
    The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU) EMA evaluates applications for marketing authorisation submitted via the centralised procedure, monitors the safety of medicines across their lifecycle and provides information to healthcare professionals and patients
  • Human regulatory: overview | European Medicines Agency (EMA)
    Information on the regulation of medicines for human use in the European Union (EU), with a focus on the centralised procedure The European Medicines Agency (EMA) plays a key role in this procedure
  • What we do - European Medicines Agency (EMA)
    The European Medicines Agency (EMA) fosters scientific excellence in the evaluation and supervision of medicines This benefits public and animal health in the European Union (EU)
  • What’s new - European Medicines Agency (EMA)
    Find all new and updated information published on our website in one place below Filters are available to narrow results down based on your interests, such as whether it relates to human or veterinary medicines or specific topics Information on medicines and related procedures includes a reference to relevant substances: INN or common name, active substance, and English common name for
  • Scientific guidelines - European Medicines Agency (EMA)
    The European Medicines Agency's Committee for Medicinal Products for Human Use prepares scientific guidelines in consultation with regulatory authorities in the European Union (EU) Member States, to help applicants prepare marketing authorisation applications for human medicines Guidelines reflect a harmonised approach of the EU Member States and the Agency on how to interpret and apply the
  • Search | European Medicines Agency (EMA)
    EMA traineeship programme informative session Join this information session and learn how to apply to the EMA traineeship Online European Medicines Agency, Amsterdam, the Netherlands
  • EMA - Scientific Explorer
    EMA's Scientific Explorer provides resources and guidance for scientific research, medicine development, and regulatory processes in the European Union
  • National registers of authorised medicines - European Medicines Agency . . .
    The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet
  • Marketing authorisation | European Medicines Agency (EMA)
    The European Medicines Agency (EMA) is responsible for the scientific evaluation of centralised marketing authorisation applications (MAA) Once granted by the European Commission, the centralised marketing authorisation is valid in all European Union (EU) Member States, Iceland, Norway and Liechtenstein





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