Evaluation of Legal Legislation Compliance and Readability of Clinical Trial Informed Consent Forms-Reference-Cited by-同舟云学术

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Evaluation of Legal Legislation Compliance and Readability of Clinical Trial Informed Consent Forms

Published:2020-01-08 Issue:2 Volume:54 Page:468-475
ISSN:2168-4790
Container-title:Therapeutic Innovation & Regulatory Science
language:en
Short-container-title:Ther Innov Regul Sci

Author:

Gungor Buket,Aylin Mualla,Asena Ayse,Somuncuoglu Elif Inci,Bozkurt Nihan Burul,Ucku Serife Reyhan,Gelal Ayse^ORCID

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Public Health, Environmental and Occupational Health,Pharmacology, Toxicology and Pharmaceutics (miscellaneous)

Link

http://link.springer.com/content/pdf/10.1007/s43441-019-00078-2.pdf

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An Example of a Clinical Research Ethics Committee in Türkiye: Types of Studies Analysed, Their Phases and Investigators;Journal of Empirical Research on Human Research Ethics;2024-08-09

2. Regulatory compliance and readability of informed consent forms in industry-sponsored drug development clinical trials;Clinical Trials;2023-05-16

3. Is the informed consent form only a symbolic document in clinical trials?;Archives of Pharmacy and Pharmaceutical Sciences;2022-12-19

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