From: Teller, Alan
[at2059@mail.cumc.columbia.edu]
Sent: Friday, September 17, 2010
10:45 AM
To: cuhs-irb@CUMC.COLUMBIA.EDU
Subject: IRB 101: September 28, 2010
The Columbia University
IRB invites you to attend our upcoming "IRB 101" seminar. The intent
of this session is to provide basic information about the history of human
subjects protection, regulatory requirements, submission tips, and RASCAL updates
as they relate to the Human Research Protection Program at CU.
Date: Tues., September 28,
2010
Time: 10:00 a.m. - 2:00
p.m.
Place: Amphitheatre A-1,
Columbia University Medical Center, 630 W. 168th Street
This session will provide:
- A history of human subjects
protection and the ethical principles that guide human subjects research;
- An overview of the
federal regulations for the protection of human subjects in research;
- Criteria for IRB review;
- Tips for submitting
complete and understandable new protocols, modifications, renewals and adverse
event reports;
- Tips for obtaining IRB
approval more quickly;
- The RASCAL system;
- The IRB review process.
Who should attend?
- Research personnel who
have not attended the IRB 101 series in the past;
- Individuals new to the
research environment;
- Research personnel new
to Columbia;
- All those who wish to
gain a historical perspective and learn the ethical and regulatory guidelines
for Human Subjects Research.
Beverages and a light
lunch will be provided.
Please RSVP to the
following link so we can plan accordingly: https://calendar.columbia.edu/sundial/webapi/register.php?eventID=43602
For current policies, applicable
regulations, meeting schedules, educational event listings, Frequently Asked
Questions, and more, please visit the CUMC IRB web site: http://www.cumc.columbia.edu/dept/irb/.
This message has been sent
by the Columbia University Institutional Review Board.
CUMC (Medical Center) IRB:
212.305.5883
www.cumc.columbia.edu/dept/irb
CU-MS (Morningside) IRB:
212.851.7040
"The Society of
Clinical Research Associates (SoCRA - www.SoCRA.org)
accepts documentation of candidate participation in continuing education programs
for re-certification if the program is applicable to clinical research
regulations, operations or management, or to the candidate's clinical research
therapeutic area. This program offers 3.5 hours of CE credit."