Entrez un mot ou une phrase dans n'importe quelle langue 👆
Langue:
Traduction et analyse de mots par intelligence artificielle ChatGPT
Sur cette page, vous pouvez obtenir une analyse détaillée d'un mot ou d'une phrase, réalisée à l'aide de la meilleure technologie d'intelligence artificielle à ce jour:
- comment le mot est utilisé
- fréquence d'utilisation
- il est utilisé plus souvent dans le discours oral ou écrit
- options de traduction de mots
- exemples d'utilisation (plusieurs phrases avec traduction)
- étymologie
FDA$27628$ - traduction vers néerlandais
US FDA DESIGNATION FOR INVESTIGATIONAL DRUGS
FDA Fast Track; Fast Track Designation; FDA Fast Track Development Program; Fast Track (FDA); Fast track status; Fast track designation
FDA
voedsel en medicijnen administratie (amerikaans)
US Food and Drug Administration
.jpg?width=200)
 (9759352093).jpg?width=200 "FDA scientist prepares blood donation samples for testing.")
 (7184535293).jpg?width=200 "Medical Officer Alexander Fleming, M. D., examines a portion of a 240-volume new drug application around the late 1980s. Applications grew considerably after the efficacy mandate under the 1962 Drug Amendments.")
.jpg?width=200 "alt=")
.jpg?width=200 "alt=")
.jpg?width=200 "FDA lab at Building 64 in Silver Spring, Maryland")
.jpg?width=200 "alt=")
![[[Harvey W. Wiley]], chief advocate of the Food and Drug Act](https://commons.wikimedia.org/wiki/Special:FilePath/Portrait of Dr. Harvey W. Wiley (FDA 107) (8203830456).jpg?width=200 "[[Harvey W. Wiley]], chief advocate of the Food and Drug Act")
![Jefferson, Arkansas]] is the headquarters of the National Center for Toxicological Research.](https://commons.wikimedia.org/wiki/Special:FilePath/Toxicology Research at FDA (NCTR Campus) (6023336064).jpg?width=200 "Jefferson, Arkansas]] is the headquarters of the National Center for Toxicological Research.")
AGENCY OF THE US DEPARTMENT OF HEALTH AND HUMAN SERVICES
FDA; United States Food and Drug Administration; US Food and Drug Administration; Product licensing application; Food and drug administration; Bureau of Chemistry; USFDA; Fda; Food & Drug Administration; Food and Drug Adminstration; ODE IV; American Food and Drug Administration; US FDA; FDA approval; FDA drug approval & regulation; U.S. Food & Drug Administration; U.S. Food and Drug Administration; The Food and Drug Administration (FDA or USFDA); Food and Drug Administration (FDA or USFDA); FDA Regulation; Food and Drug Administration (United States); USA Food and Drug Administration; United States Food And Drug Administration; U S Food and Drug Administration; Food and Drugs Administration; Pediatric exclusivity; Food and Drug Administration (US); Food, Drug, and Insecticide Administration; Taha Kass-Hout; United States Food & Drug Administration; USA FDA; U. S. Food and Drug Administration; United states food and drug administration; Federal Drug Administration; U.S. FDA; US food and drug administration; The Real Cost; Fda.gov; Food and Drugs Authority
US Voedsel en Medicijn Administratie (FDA)
nutritional information
.jpg?width=200 "FDA Commissioner Margret Hamburg speaks at a White House event regarding proposed updates to the FDA's Nutrition Facts labels for food packaging. Feb. 27, 2014")
LABEL REQUIRED ON MOST PACKAGED FOOD IN MANY COUNTRIES
Nutritional facts label; Nutrition Facts; Nutritional information; Nutritional facts; Nutrition label; Nutrition labeling; Nutrition facts; Nutrition labelling; Nutrition information; Nutrient Label; Nutrition information panel; FDA nutrition label; Nutrition Facts label; Nutrition Facts labels; Food nutrition label; Nutrition facts labelling; Nutri-Grade
voedingsinformatie (voedingstabel)
Définition
FDA
¦ abbreviation (in the US) Food and Drug Administration.
Wikipédia
Fast track (FDA)
Fast track is a designation by the United States Food and Drug Administration (FDA) of an investigational drug for expedited review to facilitate development of drugs that treat a serious or life-threatening condition and fill an unmet medical need. Fast track designation must be requested by the drug company. The request can be initiated at any time during the drug development process. FDA will review the request and attempt to make a decision within sixty days.
