z-logo
open-access-imgOpen Access
Analysis of regulatory-ethical framework of clinical trials
Author(s) -
Andrijana Milošević-Georgiev,
Dušanka Krajnović,
Srdjan Milovanović,
Svetlana Ignjatović,
Dušan Djurić,
Valentina Marinković
Publication year - 2013
Publication title -
srpski arhiv za celokupno lekarstvo
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.135
H-Index - 17
eISSN - 2406-0895
pISSN - 0370-8179
DOI - 10.2298/sarh1310659m
Subject(s) - beneficence , clinical trial , medicine , documentation , autonomy , legislature , economic justice , engineering ethics , desk , informed consent , alternative medicine , law , political science , pathology , computer science , programming language , engineering
Every clinical trial has to meet all ethical criteria in addition to the scientific ones. The basic ethical principles in the clinical trials are the following: nonmaleficence, beneficence, respect for autonomy and the principle of justice.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here