What specific electronic signatures and compliance certifications are required on initial IRB research protocol submissions for clinical trials in New Orleans medical centers?
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The searches the AI actually ran for this prompt.
SEED QUERY
What specific electronic signatures and compliance certifications are required on initial IRB research protocol submissions for clinical trials in New Orleans medical centers?
4 real searches · 1 real-search pass
New Orleans medical center IRB initial submission electronic signature investigator certification Tulane LSUHSC Ochsner LCMCGoogle ↗
OBSERVEDInstruction
Tulane IRB electronic submission initial protocol signatures CITI GCP COI certificationGoogle ↗
OBSERVEDInstruction
LSUHSC New Orleans IRB initial submission electronic signature investigator assurance training requirementsGoogle ↗
OBSERVEDInstruction
Ochsner IRB initial submission electronic signature protocol submission requirements CITI GCPGoogle ↗
OBSERVEDInstruction
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Query classes
Google's semantic query class for every sub-query: what kind of answer each search is after, simulated vs real.
ChatGPT real searches (4)
Classes come from the query-classifier (a local Laya model). 3 of 4 calls are low-confidence (under 50%) — hover a query in the table to see its confidence.
Searches and sources
ChatGPT4 real searches · gpt-6
New Orleans medical center IRB initial submission electronic signature investigator certification Tulane LSUHSC Ochsner LCMC Google ↗
Tulane IRB electronic submission initial protocol signatures CITI GCP COI certification Google ↗
LSUHSC New Orleans IRB initial submission electronic signature investigator assurance training requirements Google ↗
Ochsner IRB initial submission electronic signature protocol submission requirements CITI GCP Google ↗
- IRBManager · research.tulane.edu
- CITI Training · research.tulane.edu
- Required Trainings & Documents · medicine.tulane.edu
- Clinical Trial Checklist · research.tulane.edu
- Training: LSUHSC-NO Investigators · s.lsuhealth.com
- Full Board Research · lsuhsc.edu
- IRB Information | Human Research Protection Program · research.ochsner.org
- Collaborating with Local Institutions · s.lsuhealth.com
- Frequently Asked Questions – Statement of Investigator (Form FDA 1572) Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors · fda.gov
- Frequently Asked Questions – Statement of Investigator (Form FDA 1572) Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors · fda.gov
- Financial Disclosures by Clinical Investigators · fda.gov
- Clinical Trial Forms · fda.gov
- Electronic Systems, Electronic Records, and Electronic Signatures in Clinical Investigations: Questions and Answers · fda.gov
Queries
4 queries · click a column to sort
| Query / type | Search | Intent | Query class | Routing format | Cluster | Freq ↓ | Weight |
|---|---|---|---|---|---|---|---|
New Orleans medical center IRB initial submission electronic signature investigator certification Tulane LSUHSC Ochsner LCMC OBSERVED | Google ↗ AI Mode ↗ | — | Instruction | — | — | 1x of 1 | |
Tulane IRB electronic submission initial protocol signatures CITI GCP COI certification OBSERVED | Google ↗ AI Mode ↗ | — | Instruction | — | — | 1x of 1 | |
LSUHSC New Orleans IRB initial submission electronic signature investigator assurance training requirements OBSERVED | Google ↗ AI Mode ↗ | — | Instruction | — | — | 1x of 1 | |
Ochsner IRB initial submission electronic signature protocol submission requirements CITI GCP OBSERVED | Google ↗ AI Mode ↗ | — | Instruction | — | — | 1x of 1 |