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Compliance, regulation, and adequate protection of human subjects and the institution are our collective responsibility. To continue to enhance our professional experience and expertise and to further improve our content knowledge and job performance, please refer to the following FREE online courses and read the following material regarding human subject research:

Online Courses:
Comprehensive Course in the Protection of Human Subject Research
NIH GCP Training (free online course)

Reading Materials:
The Belmont Report
Federal Wide Assurance
FDA Policy on Informed Consent
FDA Guidance for IRB and Clinical Investigators
Information About Western IRB
WIRB Guide for Researchers
Code of Federal Regulations
FDA Good Clinical Practice 2012 Reference Guide