Office of
Regulatory Affairs
Human Research
Protection Program
2007 Fall
Using
the Flexibility Built into the IRB
Regulations:
Benefits
to IRBs and Investigators
Friday,
October 19, 2007
8:30
A.M. – 4:30 P.M.
MSU
Union,
KEYNOTE
SPEAKER
We are pleased to announce that Charles McCarthy, Ph.D., Adjunct Faculty, Office of Research, Virginia Commonwealth University and the 2003 recipient of the Public Responsibility in Medicine and Research (PRIM&R) Lifetime Achievement Award for Excellence in Research Ethics, will be the conference keynote speaker. Dr. McCarthy, the longest serving Director of the federal Office for Protection from Research Risks (OPRR) from 1980 - 1992, helped guide the development of the federal regulations for human research protection. To learn more about Dr. McCarthy, please visit http://www.primr.org/AboutUs.aspx?id=372 .
WHO
SHOULD ATTEND
Anyone involved in human subject
research, including faculty, students, staff, IRB
members, and IRB staff.
REGISTRATION
FEE
The registration fee is waived
for Michigan State University
(MSU) and Community Research Institutional Review Board
(
Affiliated with
MSU is defined as an MSU faculty member, staff, student or IRB member. Affiliated with
REGISTRATION
- NOW OPEN!
Online registration is
now open! To register,
please visit the human research web site, http://www.humanresearch.msu.edu/conferences.html and click on the link “Registration – Now Open Online”.
A confirmation will be emailed when
your registration is processed. The registration deadline is October
15, 2007. Please register
early, as seating is limited. If you register and are unable to attend, please
notify Kristen Burt by phone: 517-355-2180 ext. 235 or email:
IRBEducation@ores.msu.edu. Please feel free to contact Kristen Burt with any
questions.
SESSIONS
The agenda for the 2007 Fall IRB Educational Conference includes a plenary morning session and two afternoon breakout sessions. Please note that the tentative agenda is posted on the conference website, http://www.humanresearch.msu.edu/conferences.html. During the morning plenary session, keynote speaker Dr. Charles McCarthy will give two presentations and participate in a Q&A session. In the afternoon, participants will have a choice of breakout sessions to attend.
Breakout Session 1 - 1:15 P.M. - 2:30 P.M.
IRB Basics 1: This workshop, designed for new
IRB members, provides an introduction to human
subjects’ research protections including a historical perspective, and overview
of the regulations and techniques for completing project
reviews.
Maximizing the
Appropriate Use of Exempt and Expedited Review Categories:
When can research be exempt? When
can research be expedited? A discussion of these review categories will be
provided, highlighting the similarities, differences, and distinguishing
characteristics. This session will show you how to maximize use of these
categories in an appropriate and regulatory compliant way. Criteria that exclude
projects from exempt or expedited review will also be discussed.
Recent
OHRP
Compliance Letters: What Can We Learn?
This session provides an overview
of recent OHRP compliance determination letters, with
an emphasis on what lessons you can learn. Potential trends and common issues
among institutions will be discussed.
Waiver of Parental Permission: When is it Allowed? What is a waiver of parental permission? Under what conditions may an IRB grant such a waiver? This session will address these questions and others raised by waivers of parental permission, as well as highlighting other applicable laws, such as the Protection of Pupil Rights Amendment (PPRA). Examples of situations where waiver of parental permission may be granted will be discussed.
Breakout Session 2 - 2:45 P.M. - 4:00 P.M.
Exceptions
to Signed Consent: Waiver of Consent and Waiver of Documentation:
When can the requirement to obtain
consent or to obtain a signed consent document be
waived? This session will discuss
the criteria under which such requirements may be waived, as well as discussing
terms in the criteria, such as “impracticable.” The recent SACHRP recommendations will be highlighted.
IRB
Basics 2: This session is a continuation of
IRB Basics 1 and includes a mock review of an IRB application by
participants.
Legal
Perspectives: A Discussion of
Using
the Flexibility of the Regulations in Social Science Research:
How can we use the flexibility
built into the regulations in social science research? Areas such as defining
human subject research, using exempt and expedited review categories, and
waiving consent, parental permission
and documentation of consent will be highlighted.
CONTACT
PERSON
For answers to questions about
the 2007 Fall IRB Educational Conference, please
feel free to contact Kristen Burt, Educational Program Coordinator by phone:
(517) 355-2180 ext. 235 or email:
IRBEducation@ores.msu.edu.
Our
Mailing List
If you do not wish to receive this newsletter, please
email IRBEducation@ores.msu.edu or email me back and we will remove you from our list. If there are
other colleagues or students who you think should be on my mailing list, please
forward this email along to them and have them reply to me so I can add
them.