Ena Slavkovic
Yugoslavia
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Ena’s Selected Translation Work
Terms and text shown below represent Ena’s contributions to TermWiki.com, a free terminology website and knowledge resource for the translation community.
approved drugs
In the U.S., the Food and Drug Administration (FDA) must approve a substance as a drug before it can be marketed. The approval process involves several steps including pre-clinical laboratory and animal studies, clinical trials for safety and efficacy, filing ...
odobreni lekovi
U Sjedinjenim Državama, Zavod za zaštitu zdravlja (FDA) mora odobriti supstancu kao lek pre nego bude pušten na tržište. Ovaj proces podrazumeva nekoliko stadijuma uključujući prekliničke laboratorijske studije i studije na životinjama, kliničko testiranje ...
phase i trials
Initial studies to determine the metabolism and pharmacologic actions of drugs in humans, the side effects associated with increasing doses, and to gain early evidence of effectiveness; may include healthy participants and/or patients.
Prva faza ispitivanja
Početne studije sa ciljem određivanja metabolizma i farmakološkog dejstva lekova na čoveka, neželjena dejstva vezana za povećane doze, kao i sticanja ranog uvida u efikasnost leka; može uključiti ispitanike bez zdravstvenih problema odnosno ...
personal file access policy
A policy allowing current and prior employees access to their own files, provided they let HR know in advance.
Politika pristupa ličnim fajlovima
Politika koja dozvoljava sadašnjim i ranijim zaposlenima pristup svojim fajlovima, pod uslovom da unpared o tome obaveste menadžera za ljudske resurse.
Nevirapine
a prescription drug used to treat HIV-positive adults who show immulogical deterioration
Nevirapine
lek koji se koristi u lečenju odraslih koji su HIV pozitivni sa deterioracijom imunog sistema
pharmaceuticals
Chemical substance for medical purposes, including diagnosis, treatment and prevention of disease.
lekovi
Hemijska supstanca koja se koristi u medicinske svrhe, uključujući dijagnostiku, lečenje ili prevenciju bolesti.
modularization
Teaching process that splits material or courses into modules to allow students flexibility in selecting modules to create a program of study.
modularizacija
Obrazovni proces koji razdvaja materijal ili kurseva na module čime se studentima omogućava felksibilnost u izabirz modula priliko kreiranja programa studiranja.
Food and Drug Administration
The U.S. Department of Health and Human Services agency responsible for ensuring the safety and effectiveness of all drugs, biologics, vaccines, and medical devices, including those used in the diagnosis, treatment, and prevention of HIV infection, AIDS, and ...
Administraija za hranu i lekove
Deo američkog Zavoda za Zdravlje i Zdravstvene Usluge odgovoran za obezbeđivanje bezbednosti i efikasnosti svih lekova, bioloških preparata, vakcina i medicinskih sredstava, uključujući one koji se koriste u dijagnostici, lečenju i prevenciji HIV-a, AIDS-a ...
phase iii trials
Expanded controlled and uncontrolled trials after preliminary evidence suggesting effectiveness of the drug has been obtained, and are intended to gather additional information to evaluate the overall benefit-risk relationship of the drug and provide and ...
Treća faza ispitivanja
Proširena kontrolisana i nekontrolisana ispitivanja posle preliminarne evidencije kojom je postignuta efikasnost leka i kojom se namerava prikupljanje dodatnih informacija za procenu sveukupnog odnosa korist-rizik leka i omogući adekvatna osnova za lekara ...
Family and Medical Leave Act
This act stipulates that employers must provide up to 12 weeks of unpaid leave to eligible employees.
Zakon o porodičnom i zdravstvenom odsustvu
Ovaj zakon nalaže da poslodavci moraju omogućiti najviše 12 nedelja neplaćenog odsustva kvalifikovanim zaposlenima.
data safety and monitoring board (dsmb)
An independent committee, composed of community representatives and clinical research experts, that reviews data while a clinical trial is in progress to ensure that participants are not exposed to undue risk. A DSMB may recommend that a trial be stopped if ...
Odbor za bezbednost podataka i monitoring
Nezavisni odbor koji se sastoji od predstavnika udruženja i stručnjaka za klinička ispitivanja koji vrše pregled podataka u toku samog kliničkog ispitivanja radi sigurnosti da učestnici nisu izloženi nepotrebnom riziku. ovaj Odbor(DSMB)može predložiti ...
