Archived documents

Documents past their public comment period for Biomedical Research.

FDARFI

Drug Repurposing for Unmet Medical Needs; Request for Information

608 comments

Net support +95% across analyzed comments

Top issues in comments

  • Drug repurposing for long covid
  • Expand fda-approved indications
  • Treatment for long covid
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FDARFI

AI-Enabled Optimization of Early- Phase Clinical Trials Pilot Program; Request for Information

239 comments · 2 awaiting analysis

Net support +94% across analyzed comments

Top issues in comments

  • Ai-enabled clinical trial optimization
  • Standardized evaluation framework
  • Ai bias and healthcare equity
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FDAOther

Protocol Deviations for Clinical Investigations of Drugs, Biological Products, and Devices; Guidance for Industry - Draft Guidance

55 comments

Net support +60% across analyzed comments

Top issues in comments

  • Classification of protocol deviations
  • Reporting responsibilities for deviations
  • Guidance specificity and rigor
Read the record →Closes Mar 1
FDAOther

Quantitative Systems Pharmacology (QSP)-Based Dose Selection for Minimum Anticipated Biological Effect Level (MABEL) in First-inHuman (FIH) Trials; Guidance for Industry; Draft Guidance

6 comments · 5 awaiting analysis

Net support 0% across analyzed comments

Top issues in comments

Not yet determined
Read the record →Closes Jul 25
CDCNotice

Focus on Advancing Support and Transition with the Fragile X Online Registry with Accessible Research Database (FAST FORWARD)

2 comments

Net support +50% across analyzed comments

Top issues in comments

  • Funding for fxs activities
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FDANotice

Advancing the Use of Digital Health Technologies in Clinical Investigations for Drugs and Biological Products; Request for Information and Comments

1 comment

Net support +100% across analyzed comments

Top issues in comments

  • Qualification of digitally-derived endpoints
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FDARFI

Biomarker Incubator: Urinary Kidney Safety Biomarkers; Request for Information

1 comment

Net support +100% across analyzed comments

Top issues in comments

  • Pediatric and neonatal considerations
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FDAOther

Psychedelic Drugs: Considerations for Clinical Investigations; Guidance for Industry; Draft Guidance

0 comments

Analysis in progress

Top issues in comments

Not yet determined
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FDAOther

Cancer Clinical Trial Eligibility Criteria: Washout Periods and Concomitant Medications; Guidance for Industry, IRBs, and Clinical Investigators - Draft Guidance

0 comments

Analysis in progress

Top issues in comments

Not yet determined
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FDAOther

Cancer Clinical Trial Eligibility Criteria: Performance Status; Guidance for Industry, IRBs, and Clinical Investigators - Draft Guidance

0 comments

Analysis in progress

Top issues in comments

Not yet determined
Read the record →
FDAOther

Cancer Clinical Trial Eligibility Criteria: Laboratory Values; Guidance for Industry, IRBs, and Clinical Investigators - Draft Guidance

0 comments

Analysis in progress

Top issues in comments

Not yet determined
Read the record →