IRB Insights: Tips for Submission to the Institutional Review Board

The institutional review board (IRB) is an essential collaborator in the pediatric research process. Research must be scientifically and ethically sound to produce meaningful results, and it is the IRB's responsibility to review and approve human subjects' research while protecting the subjects' rights, minimizing research risks, and maximizing the benefits. Understanding the research approval process is important for any clinician investigator hoping to conduct human subjects' research. Although IRB requirements can, and often do, vary by site, there are important overarching requirements that apply to all institutions. We aim to provide general, practical guidance on how to navigate a study through the IRB process in 3 sections: what to consider before starting your study documents, what to consider while drafting documents, and what happens after you submit. Our hope is that these helpful hints lead to efficient IRB review of proposed research and successful science.

Authors

Institutions

Publication Details

Journal
Hospital Pediatrics
Published
2025-08-22
DOI
https://doi.org/10.1542/hpeds.2025-008403
Primary Topic
Ethics in Clinical Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

IRB Insights: Tips for Submission to the Institutional Review Board

Hadley S. Sauers‐Ford, Allison M. Wiedeman, Benjamin Rocky Byington, Saima Deen
Hospital Pediatrics
Ethics in Clinical Research
article

IRB Insights: Tips for Submission to the Institutional Review Board

Hadley S. Sauers‐Ford, Allison M. Wiedeman, Benjamin Rocky Byington, Saima Deen
article en

Abstract

The institutional review board (IRB) is an essential collaborator in the pediatric research process. Research must be scientifically and ethically sound to produce meaningful results, and it is the IRB's responsibility to review and approve human subjects' research while protecting the subjects' rights, minimizing research risks, and maximizing the benefits. Understanding the research approval process is important for any clinician investigator hoping to conduct human subjects' research. Although IRB requirements can, and often do, vary by site, there are important overarching requirements that apply to all institutions. We aim to provide general, practical guidance on how to navigate a study through the IRB process in 3 sections: what to consider before starting your study documents, what to consider while drafting documents, and what happens after you submit. Our hope is that these helpful hints lead to efficient IRB review of proposed research and successful science.

Hospital PediatricsVol. 15(9)
Cincinnati Children's Hospital Medical Center (US), Texas Children's Hospital (US)
Peace, Justice and strong institutions
Openalex Percentile: Top 70%
Ethics in Clinical Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

IRB Insights: Tips for Submission to the Institutional Review Board — Hadley S. Sauers‐Ford, Allison M. Wiedeman, et al. · Hospital Pediatrics (2025) | TGRS Research Map | TGRS