Showing results for IRB

The Benefits of Data Sharing and its Contribution to Research Transparency
Overview As digital technologies become cheaper and more powerful, the storing, analysis, and transfer of the raw output of scientific inquiry become...
Upcoming Podcast Updates: Here's What You Need to Know
Introduction As we enter the new year, we are thrilled to begin the second season of our podcasts, On Campus and On Research. They have undergone a m...
NIH Seeks Input on Developing Consent Language for Digital Health Research
Introduction In recent years, digital health technologies have revolutionized biomedical and behavioral research, offering new possibilities for scie...
FDA-Regulated Research
Addresses U.S. Food and Drug Administration-regulated clinical research and the responsibilities of researchers, IRBs, and sponsors when an FDA-regula...
Internal Quality Assurance and Quality Improvement of the HRPP
Provides a general overview of how a HRPP quality assurance/quality improvement (QA/QI) audit program may be structured and why, and focuses on two co...
Recognizing and Reporting Unanticipated Problems Involving Risks to Subjects or Others in Biomedical Research
The U.S. Food and Drug Administration and the U.S. Department of Health and Human Services human subject protection regulations require institutions t...
Gender and Sexuality Diversity (GSD) in Human Research
Provides a starting point to develop cultural competency for human subject researchers and research team members, who will come in contact with subjec...
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