Thomas Jefferson University

IRB Member Continuing Education

IRB Member continuing education sessions are presented regularly at IRB meetings. The presentations appear below, starting with the most recent.

Description Date(s) Presented

The Lessons of History Feb, Mar 2021
Research in the Operating Room Feb, Mar 2021

Considerations for IRB Review of Cell Based Therapies Dec 2020
Informed Consent Format Update
Feb 2020

Payment to Participants - A Case Study Oct, Nov 2019
IRB Review Sep, Oct 2019
Informed Consent/Subject Injury Update Jun, Jul 2019
Sponsor-Initiated Investigational Drug Applications (INDs) May 2019
Cannabis Research Information for Jefferson IRBs Apr 2019
MCARE and Consent - Refresher Mar, Apr 2019
Confidentiality Agreements Feb 2019

New Continuing Review Provisions under Revised Common Rule: Forms & SOP Oct, Nov 2018
June 2018 FDA Inspection of IRB Oct, Dec 2018
Drug Development Stages Sep, Oct 2018
Children as Subjects – Important Ethical and Logistical Considerations Aug 2018
A survey into the implementation of commercial IRBs at TJU and their impact on the workload of the local IRB Jul 2018
Medicated Assisted Treatment for Opiate Addiction Jun 2018
News from Denver: AHHRPP Conference 2018 May 2018
Adolescents and IRBs Mar, Apr 2018
PA Court Ruling on Consent Feb 2018 
Common Rule Changes to Consent and Template Jan 2018 

Consolidation of IRB Review Nov 2017 
Basic Pharmacokinetics Oct 2017 
Oncology Clinical Trials Aug, Sep 2017
COI and Human Research Jun, Jul 2017
Consent Coercion Creep May, Jul 2017
Community Based Participatory Research Apr, May, Jun 2017
Common Rule Revision Feb 2017
Consent Signatories Jan 2017

Introduction to Export Control Oct, Nov 2016
Sponsor Expectations for Clinical Studies Sep, Oct 2016
Community Outreach Jul, Aug, Sep 2016
IRB Full Review Voting Guidance Jun 2016
AAHRPP Site Review Feedback May 2016
Data Gathering Activities that Do Not Constitute Human Subjects Research Mar, Apr 2016
Department of Defense (DoD) Funded Human Subjects Research Feb, Mar 2016
The TJU HRPP Part II Jan, Feb 2016
The TJU HRPP Part I Jan 2016

Community Based Participatory Research Oct, Nov 2015
Consent Form Readability Sep 2015
Drug Development and IND Process Aug 2015
Review of New IRB Policies Jun 2015
Pharmacy & The IRB May 2015
Deception in Human Subjects Research Apr 2015
Risks of Standard of Care in Consent Forms Feb 2015
HUD and Emergent Use Jan 2015

Avenues of Consent Feb 2015
Dec 2014
Non-Compliance Nov 2014
HIPAA Breach Notification Sep 2014
Quality Improvement Activities Jul, Aug 2014
Levels of Review Jun, Jul 2014
Exploring 45 CFR 46.111 May 2014
Regulatory Guidance for Genetic Testing Apr 2014