IRB Conferences, Education & Orientation

All UMDNJ faculty, students, and other individuals involved in human subjects research are welcome to attend any of our upcoming IRB events and education sessions. Please continue to monitor this page for upcoming events.

Conferences and Events

 

Check Back for Upcoming Events

We update our events section as new updates become available. Please check back to view our upcoming events

"Basics for Informed Consent in Research"
This session will cover several key topics instrumental to understanding the consent
process in human subjects' research:

  • Overview of the ethical principles underlying informed consent
  • Current regulatory requirements
  • Common findings by auditors
  • The subject's view of the consent process

Date and Time: April 4, 2012 9:30 a.m. – 11:30 a.m.
Location:
UMDNJ- New Brunswick Campus
Cancer Institute of New Jersey
195 Little Albany Street
Auditorium A

Please click on the link below for more information:

Basics for Informed Consent

eIRB Training Sessions:

eIRB is the new web-based application routing and tracking system. The system will increase the efficiency of the approval and administrative processes for projects and protocols involving human subjects in research. It is designed to replace the cumbersome and paper-intensive process under which applicants currently apply for IRB approval of study proposals. eIRB has been developed to standardize and computerize the Institutional Review Boards (IRBs) at UMDNJ.

Training dates are available here.

Date Event
12/21/2011 Understanding the Various Types of IRB Review:
Non-Human Subject, Exempt, Expedited, Facilitated,
Full Board, and Quality Assurance - Piscataway
11/17/2011 Understanding the Various Types of IRB Review:
Non-Human Subject, Exempt, Expedited, Facilitated,
Full Board, and Quality Assurance - Stratford
11/1/2011 Understanding the Various Types of IRB Review:
Non-Human Subject, Exempt, Expedited, Facilitated,
Full Board, and Quality Assurance - New Brunswick
10/26/2011 Webinar: How to survive an FDA Inspection
10/7/2011 Understanding the Various Types of IRB Review:
Non-Human Subject, Exempt, Expedited, Facilitated,
Full Board, and Quality Assurance - Newark
4/14/2011 "Ask the IRB Informational Sessions" - Stratford Campus
4/5/2011 "Biobanking Basics: An Overview of Current Legal and Compliance Issues Related to Human Specimens Collected in Reseach"
3/30/2011 "Ask the IRB Informational Sessions" - Newark Campus
3/29/2011 "Ask the IRB Informational Sessions" - Piscataway
3/18/2011 "Ask the IRB Informational Sessions" - New Brunswick Campus
2/15/2011 "Form 483 and Warning Letter Responses: Critical Component of the FDA's Evolving "Get Tough" Enforcement"
Nov. 20, Dec. 7 & Dec. 10, 2009 Investigators’ Responsibilities for Protecting the Rights, Safety and Welfare of Study Subjects
Read FDA Final Guidance (10/2009)
Dec 2 - 18, 2008 Understanding the New Surrogate Consent Process
NJ Statute: Access to Medical Reseach Act
Sept 17 - 19, 2008 Privacy, Confidentiality and Data Security in Research
Download Slides

6/19/2008
4/18/2008
4/11/2008

Hot Topics in Human Subject Research:
1/30/2008

Device Workshop
9/20/2007

Social, Behavioral & Epidemiologic Research (Stratford Campus)
8/22/2007 New IRB Application and Forms - New Brunswick
7/30/2007 New IRB Application and Forms - Piscataway
7/24/2007 New IRB Application and Forms - Newark
7/19/2007 New IRB Application and Forms - Stratford
7/12/2007 New IRB Application and Forms - New Brunswick
6/21/2007

Social, Behavioral & Epidemiologic Research

3/13/2007 Annual IRB Retreat
Tissue and Data Repositories: Issues & IRB Concerns