The IRB presents a new webinar on the second Thursday of every month during the academic calendar year.  The presentations start at 12 pm and typically last about 30 minutes. See below for specific dates and topics that will be presented. Following the live presentation, the recording of the webinar and Q&A session will be archived for easy access. Every webinar has its own survey to provide your feedback and ideas for future webinars, which may be accessed at any time.

If you have any questions about the webinars, or would like to recommend a topic, please contact Maria Davila at maria.davila@emory.edu

2019 Webinars

Access Title Date Survey
Watch Recording or Access Slides Informed Consent: Concise Presentation of Key Information 2/14/2019 Link
Watch Recording Q&A With the IRB 1/10/2019 Not active


2018 Webinars

Access Title Date Survey
Watch Recording or access the Slides Common Rule Implementation Plan-Latest Information 12/13/2018 Link
Watch Recording or access Slides

Common Rule Implementation and Emory- 2 of 2

11/8/2018 Link
Watch Recording or access  Slides

Common Rule implementation and Emory- 1 of 2

10/11/2018 Link
Watch Recording

Emory + Children’s Pediatric Institute Overview

9/13/2018 Link
Watch Recording

Electronic Data: Security Concerns in Research

5/10/2018 Link
Watch Recording

All Things Reliance: Using a Single IRB and Other Emory Processes for Multi-Site Studies

4/12/2018 Link
Watch Recording

Expanded Access to Investigational Drugs and Devices: Emory IRB’s Revised Review Procedures

3/8/2018 Link
Watch Recording

Common Rule Changes for Informed Consent: Plans for Implementation

2/8/2018 Link
Watch Recording

Summary of Changes to the Common Rule and NIH Single IRB Policy

1/11/2018 Link

2017 Webinars

Access Title Date Survey
Watch Recording

How to Share:  The Nuts and Bolts of Human Subject Data Transfers

11/9/2017 Link
Watch Recording

Reportable Events at Continuing Review: What do I need to submit to the IRB?

10/12/2017 Link
Watch Recording Upcoming Changes Affecting Human Subjects' Research: Single IRB, Common Rule and NIH updates 9/14/2017 Link
Watch Recording Changes in Study  Procedures or Funding: is a new study needed? (slides) 8/10/2017 Link
Watch Recording Subject Complaints: what to report to the IRB 5/11/2017 Link
Watch Recording Compensation in Research 4/13/2017 Link
Watch Recording Research with Children's Healthcare of Atlanta (slides)      3/9/2017 Link
Watch Recording Certificates of Confidentiality: protecting privacy and confidentiality (slides) 2/9/2017 Link
Watch Recording  Family Members as Interpreters: Review of Emory Guidance (guidance and slides 1/12/2017 Link

2016 Webinars

Access Title Date Survey
Watch Recording Social Media and Recruitment (slides) 11/10/2016 Link
Watch Recording Setting up Databases, Registries and Sample Repositories: Important Guidelines (slides) 10/13/2016 Link
Watch Recording Genetic Research: Informed consent information (slides) 9/8/2016 Link
Watch Recording Emory HIPAA policy changes affecting research (slides) 8/11/2016 Link
Watch Recording Non-human Subjects Research Determination (slides) 5/12/2016 Link
Watch Recording Closing a Study with the IRB (slides) 4/14/2016 Link
Watch Recording IRB Training Requirements (slides) 3/10/2016 Link
Watch Recording Informed Consent Process Documentation: from in-person to mail/phone informed consent process (slides) 1/14/2016 Link

2015 Webinars

Access Title Date Survey
Watch Recording Research in Prisoners and Recently Incarcerated Subjects 11/12/2015 Link
Watch Recording NPRM for Revisions to the Common Rule 10/8/2015 Link
Watch Recording Collaborative Research: Handling IRB Concerns 9/10/2015 Link 
Watch Recording International Research: General Considerations (slides) 5/14/2015 Link 
Watch Recording
Continuing Review Considerations (slides) 4/9/2015 Link

Watch Recording

Screening Procedures: What is Covered by a Partial HIPAA Waiver and What is Not (slides) 3/12/2015 Link
Download Video New Study Submissions to the IRB (slides) 2/12/2015 Link

Watch Recording

Data Breaches: Avoiding Them and What to Do If They Happen (slides) 1/8/2015 Link

2014 Webinars

Access Title Date Survey
Watch Recording

What Types of Projects Require IRB Review? (slides)

12/11/2014 Link

Watch Recording

An Overview of the ICF Process (slides) 11/13/2014 Link
Watch Recording

Single Use Expanded Access IND/IDE (slides)

10/9/2014 Link
Watch Recording Emory IRB Reporting Requirements for UPs, NC, and Protocol Deviations (slides) 9/11/2014 Link
Watch Recording Internet Research Ethics and the IRB (slides) 8/14/2014 Link
Watch Recording Research Specimen Banking (slides) 7/10/2014 Link
Watch Recording Informed Consent Documentation: How to do it right! (slides) 6/12/2014 Link
Watch Recording Getting Your ICF Approved on the First Try (slides) 5/8/2014 Link