Human Research Protections

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Training & Educational Videos

HRP Education and Guidance Videos

101 Courses: the Basics

IRB101: An Introduction to the WCM IRB (29:55)
IRB101 video IRB101 handout
REGS101: ClinicalTrials.gov (8:43)
REGS101 CT.gov video REGS101 CT.gov handout

HRP Trainings

ClinicalTrials.gov Quarterly Training 2/2/2022 (1:21:06)
CT.gov Quarterly Training video CT.gov Quarterly Training handout

IRB Guidance: Tips, Tools, and Informational Videos

The New IRB Initial Review Application (20:03)
New IRA video New IRA handout
IRB Guide: Checking Readability Scores (8:16)
Checking Readability video Checking Readability handout
The Key Information Section: A 2018 Common Rule Requirement for the Informed Consent Form (21:25)
Key Information video Key Information handout

HRP January 2024 In-person Event Sessions

Tuesday, 1/9 Sessions

Navigating WRG-HS (38:59)
Navigating WRG-HS presentation recording / Navigating WRG-HS slide handout
FAQs, Facts, & Fiction (1:09:41)
FAQs, Facts & Fiction presentation recording / FAQs, Facts, & Fiction slide handout
Life After IRB Approval (45:15)
Life After IRB presentation recording / Life After IRB slide handout
Becoming an IRB Member (21:54)
IRB Member presentation recording / IRB Member slide handout
HRPP v. IRB (17:46)
HRPP v. IRB presentation recording / HRPP v. IRB slide handout

Wednesday, 1/10 Sessions

Single IRB: How Does It Impact You? (47:16)
Single IRB presentation recording / Single IRB slide handout

Understanding the IRB Review Application (IRA) (55:07)
IRA presentation recording / IRA slide handout

Grant and IRB Crossover (53:31)
Grant and IRB Crossover presentation recording / Grant and IRB Crossover slide handout

Additional handouts from this session:

Pulling Back the Curtain: A Look Into IRB Pre-review and IRB Review (51:12)
Pulling Back the Curtain presentation recording / Pulling Back the Curtain slide handout
FDA-Regulated Research (47:38)
FDA-Regulated Research presentation recording / FDA-Regulated Research slide handout

Thursday, 1/11 Sessions

DSMC: How and When to Use (22:38)
DSMC presentation recording / DSMC slide handout
HIPAA and the IRB (48:10)
HIPAA and the IRB presentation recording / HIPAA and the IRB slide handout
How to Write an Informed Consent Form (1:03:23)
Informed Consent presentation recording / Informed Consent slide handout
Research Involving Columbia University (22:30)
Columbia presentation recording / Columbia slide handout
Common Issues on Review (37:30)
Common Issues presentation recording / Common Issues slide handout

Other Resources

...from other WCM sites

How to Amend Your Protocol in WRG

...from the Office of Human Research Protections (Health and Human Services)

Contact Us IRB Member Portal Forms, Templates & Guidelines Request a Consultation WCM/CUMC Collaborations

Weill Cornell Medicine Human Research Protections 575 Lexington Avenue New York, NY 10022 Phone: (646) 962-8200