Ohio CTSAs Implement a Reliant IRB Model for Investigator-Initiated Multicenter Clinical Trials

Author:

Cola Philip A.1,Reider Carson2,Strasser Jane E.3

Affiliation:

1. University Hospitals Case Medical Center/Clinical Translational Science Collaborative; Case Western Reserve University; Cleveland; Ohio; USA

2. The Center for Clinical & Translational Science; The Ohio State University; Columbus; Ohio; USA

3. Center for Clinical & Translational Science & Training; University of Cincinnati; Cincinnati; Ohio; USA

Publisher

Wiley

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Cited by 4 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. Institutional Review Board (IRB) Shopping- Accessible for Public Comment;International Journal of Nursing Education and Research;2021-12-01

2. Stakeholder Experiences with the Single IRB Review Process and Recommendations for Food and Drug Administration Guidance;Ethics & Human Research;2021-05

3. The SMART IRB platform: A national resource for IRB review for multisite studies;Journal of Clinical and Translational Science;2019-07-29

4. Glomerular Diseases: Registries and Clinical Trials;Clinical Journal of the American Society of Nephrology;2016-09-26

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