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 ⇄Suchrichtung
 Übersetzung für 'FDA' von Englisch nach Deutsch
SYNO FDA | Food and Drug Administration
MedTech.pharm.QM
FDA approval
FDA-Zulassung {f}
med.MedTech.pharm.
(not) FDA-approved {adj}
(nicht) FDA-zugelassen
law
FDA Bioterrorism Regulations {pl}
Bioterrorismusgesetz {n} der FDA
admin.med.pharm.
Food and Drug Administration <FDA>
Arzneimittelzulassungs­behörde {f} [USA]
FoodInd.med.pharm.
Food and Drug Administration <FDA>
FDA {f} [behördliche Lebensmittelüberwachung und Arzneimittelzulassungs­behörde der USA]
FoodInd.med.pharm.
Food and Drug Administration <FDA> [Am.]
Food and Drug Administration {f} <FDA> [kontrolliert die Sicherheit u. Wirksamkeit von Human-/Tierarzneimitteln, biolog. Produkten, Medizinprodukten, Lebensmitteln u. strahlenemittierenden Geräten]
admin.med.pharm.
Food and Drug Administration <FDA> [USA]
[US-amerikanische Behörde für Lebensmittel- und Arzneimittelsicherheit (FDA)]
7 Übersetzungen
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  • FDA {f} [behördliche Lebensmittelüberwachung und Arzneimittelzulassungsbehörde der USA] = Food and Drug Administration <FDA>
  • Fernmeldedienstanbieter {m} <FDA> [schweiz.] [Telekommunikationsdienstleister] = telecommunications service provider <TSP>
  • FDA-Zulassung {f} = FDA approval
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Anwendungsbeispiele Englisch
  • On 19 November 2008, an FDA antiinfective drug advisory committee concluded that they would recommend telavancin be approved by the FDA.
  • In 1992 FDA published "Statement of Policy: Foods derived from New Plant Varieties".
  • For drug master files, the version posted on the web is the current version. The address for submitting DMF documentation to the FDA in the Guidance is dmfquestion@cder.fda.gov.
  • Food and Drug Administration (FDA) approved it for a similar use.
  • In the early 1990s, the soft drink industry initially approached FDA with concerns about benzene formation in soft drinks.

  • It was approved by FDA on December 4, 1997. It is available in US as Omnicef by Abbott Laboratories and in India as Cednir by Abbott, Kefnir by Glenmark, Cefdair by Xalra Pharma and Cefdiel by Ranbaxy.
  • In 2001, ViroPharma submitted a New Drug Application of pleconaril to the FDA for the common cold.
  • The FDA sent Jazz an FDA warning letter about safety violations in September 2007.
  • She incorporated information from the FDA's 1933 exhibit, and from the FDA's archives, indicating that dangerous products were known and studied by the FDA.
  • The FDA generally viewed each operating instance of Nightscout as a "medical device" subject to labeling, hazard management, and FDA reporting requirements.

  • After Scott Gottlieb became FDA commissioner in 2017, the CEO of Amicus began lobbying him directly for the FDA to accept the NDA and in February 2018 the FDA accepted it and promised a response by August 2018.
  • On 31 January 2022, Novavax applied to the Federal Drug Administration (FDA) for emergency use authorization (EUA) for NVX-CoV2373, and on June 7, FDA's panel of outside advisors recommended FDA grant the EUA.
  • The command fbplot for functional boxplots is in fda R package, and MATLAB code is also available.
  • The FDA was not made aware of the Nissen meta-analysis results until the day of its publication.
  • After receiving FDA's request for additional (CMC) chemistry-manufacturing-control related information for Rolontis (eflapegrastim), Spectrum voluntarily withdrew its 2018 Biologics License Application (BLA) from FDA as more than 60 days time would have beenneeded to provide the additional CMC-related information FDA required before March 29, 2019, the end date of FDA's initial 60-day review period.

  • In 2013 FDA warned the public that Potiga (ezogabine) can cause blue skin discoloration and eye abnormalities characterized by pigment changes in the retina.
  • "FDA Consumer" was a magazine published from 1967 through 2007 by the U.S.
  • The US FDA granted NeuroVax both FDA Pediatric Orphan Designation on February 6, 2014 & FDA Fast Track Designation for SPMS.
  • The United States Food and Drug Administration (FDA) issued a FDA warning letter to Formans' on 12 May 2020; the FDA accepted the company was in compliance on 29 September 2020.
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Enthält Übersetzungen von der TU Chemnitz sowie aus Mr Honey's Business Dictionary (nur Englisch/Deutsch).
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