
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.