[Translated article] Design and validation of two instruments to analyze and evaluate the formal quality in the informed consent process of clinical trials with medicinal products-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

[Translated article] Design and validation of two instruments to analyze and evaluate the formal quality in the informed consent process of clinical trials with medicinal products

Published:2023-03 Issue:2 Volume:47 Page:T64-T68
ISSN:1130-6343
Container-title:Farmacia Hospitalaria
language:en
Short-container-title:Farmacia Hospitalaria

Author:

Jaramillo Vélez Andrea G.,Aguas Compaired Margarita,Granados Plaza Montserrat,Mariño Eduardo L.,Modamio Pilar

Publisher

Elsevier BV

Subject

Pharmacology

Reference14 articles.

1. Reglamento (UE) No 536/2014 del Parlamento Europeo y del Consejo, de 16 de abril de 2014, sobre los ensayos clínicos de medicamentos de uso humano, y por el que se deroga la Directiva 2001/20/CE,2014

2. Real Decreto 1090/2015, por el que se regulan los ensayos clínicos con medicamentos, los Comités de Ética de la Investigación con medicamentos y el Registro Español de Estudios Clínicos,2015

3. The quality of informed consent forms systematic review and critical analysis;Lühnen;Dtsch Arztebl Int,2018

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP