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  • European Medicines Agency (EMA)
    EMA concludes review of semaglutide medicines and starts review of two chickenpox vaccines
  • 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
  • About us - European Medicines Agency (EMA)
    The European Medicines Agency (EMA) is a decentralised agency of the European Union (EU) It is responsible for the scientific evaluation, supervision and safety monitoring of medicines
  • Who we are - European Medicines Agency (EMA)
    EMA aims to create an open working environment and attract a diverse workforce We strive to make people feel safe and respected, and to ensure equal access to career opportunities In 2022, EMA adopted a diversity and inclusion charter
  • What we do - European Medicines Agency (EMA)
    The mission of the European Medicines Agency (EMA) is to foster scientific excellence in the evaluation and supervision of medicines, for the benefit of public and animal health in the European Union (EU)
  • European public assessment report - European Medicines Agency (EMA)
    EMA Service Desk (system support) Services and databases European Medicines Agency Domenico Scarlattilaan 6 1083 HS Amsterdam The Netherlands Tel: +31 (0)88 781 6000 How to find us Postal address and deliveries Business hours and holidays RSS Feed Bluesky YouTube
  • 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
  • Whats new - European Medicines Agency (EMA)
    Event: EMA FVE info session for veterinary practitioners : Understanding the first report of sales and use of antimicrobials in animals Updated 05 06 2025
  • 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
  • New guideline on inclusion of pregnant and breastfeeding individuals in . . .
    EMA has released for public consultation a new guideline providing recommendations on how to include and or retain pregnant and breastfeeding people in clinical trials The goal is to ensure developers generate robust clinical data in those populations, so that these individuals and their healthcare providers can make informed, evidence-based





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