Compliance & Safety
| Resource | Category | Topic | Type |
|---|---|---|---|
Ò×ʤ²©¹ÙÍø IRB application review process flow chart.
|
Compliance & Safety | Human Subjects | Resource |
Responsibilities of directors of research studies involving human subjects.
|
Compliance & Safety | Human Subjects | Guidance |
Ò×ʤ²©¹ÙÍø IRB guidance on information individuals in Ò×ʤ²©¹ÙÍø are legally required to report.
|
Compliance & Safety | Human Subjects | Guidance |
Ò×ʤ²©¹ÙÍø IRB HIPAA sample research authorization form.
|
Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Form |
Ò×ʤ²©¹ÙÍø IRB HIPAA sample authorization language for consent forms.
|
Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Form |
Ò×ʤ²©¹ÙÍø IRB guidance on HIPAA impacts on research Involving human subjects.
|
Compliance & Safety | Health Insurance Portability & Accountability Act (HIPAA), Human Subjects | Guidance |
Ò×ʤ²©¹ÙÍø IRB guidelines for research involving children/minors.
|
Compliance & Safety | Human Subjects | Guidance |
NIH webpage on clinical trials
|
Compliance & Safety | Human Subjects | Guidance |
Ò×ʤ²©¹ÙÍø IRB guidance on privacy, confidentiality and anonymity in human subjects research.
|
Compliance & Safety | Human Subjects | Guidance |
Ò×ʤ²©¹ÙÍø IRB guidance about activities involving human subjects and Ò×ʤ²©¹ÙÍø IRB approval. Updated December 2024.
|
Compliance & Safety | Human Subjects | Guidance |
