What documents are strictly required for an IRB human subjects research protocol submission, and how can we speed up university review times?
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Fan-out diagram
The searches the AI actually ran for this prompt.
SEED QUERY
What documents are strictly required for an IRB human subjects research protocol submission, and how can we speed up university review times?
3 real searches · 1 real-search pass
US university IRB initial protocol submission required documents protocol consent recruitment materials investigator training data collection instruments officialGoogle ↗
OBSERVED
HHS OHRP Common Rule informed consent documentation IRB submission requirements 45 CFR 46 officialGoogle ↗
OBSERVED
university IRB submission checklist required documents protocol application consent CITI training officialGoogle ↗
OBSERVED
Badge and edge weight = share of passes that produced the query. Hover a query for its intent and routing format.
Query classes
Google's semantic query class for every sub-query: what kind of answer each search is after, simulated vs real.
Classifying 3 queries…
Searches and sources
ChatGPT3 real searches · gpt-6
US university IRB initial protocol submission required documents protocol consent recruitment materials investigator training data collection instruments official Google ↗
HHS OHRP Common Rule informed consent documentation IRB submission requirements 45 CFR 46 official Google ↗
university IRB submission checklist required documents protocol application consent CITI training official Google ↗
- Required Documents and Forms for IRB Applications · irb.utah.edu
- Preparing your IRB Submission - Office for Human Subject Protection · rochester.edu
- Initial Submissions · bu.edu
- Preparing & Submitting a Protocol | Research & Innovation Office · colorado.edu
- Human Subjects Research FAQs · research.utexas.edu
- What supporting documents must I include with my IRB submission?: Institutional Review Board (IRB) Office · irb.northwestern.edu
- All Required Documents for IRB Submission · resources.uta.edu
- FAQs Category: Investigator Responsibilities · hhs.gov
- Informed Consent FAQs · hhs.gov
- Institutional Review Board Written Procedures: Guidance for Institutions and IRBs (2025) · hhs.gov
- Institutional Review Board (IRB) Written Procedures: Guidance for Institutions and IRBs · hhs.gov
Queries
3 queries · click a column to sort
| Query / type | Search | Intent | Query class | Routing format | Cluster | Freq ↓ | Weight |
|---|---|---|---|---|---|---|---|
US university IRB initial protocol submission required documents protocol consent recruitment materials investigator training data collection instruments official OBSERVED | Google ↗ AI Mode ↗ | — | — | — | — | 1x of 1 | |
HHS OHRP Common Rule informed consent documentation IRB submission requirements 45 CFR 46 official OBSERVED | Google ↗ AI Mode ↗ | — | — | — | — | 1x of 1 | |
university IRB submission checklist required documents protocol application consent CITI training official OBSERVED | Google ↗ AI Mode ↗ | — | — | — | — | 1x of 1 |