טוען...
Readability and Content Assessment of Informed Consent Forms for Phase II-IV Clinical Trials in China
PURPOSE: To explore the readability and content integrity of informed consent forms (ICFs) used in China and to compare the quality of Chinese local ICFs with that of international ICFs. METHODS: The length, readability and content of 155 consent documents from phase II-IV drug clinical trials from...
שמור ב:
| הוצא לאור ב: | PLoS One |
|---|---|
| Main Authors: | , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Public Library of Science
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5049790/ https://ncbi.nlm.nih.gov/pubmed/27701471 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0164251 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|