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IRB
Brown Bag Seminars Announced
The Office for the Protection of Research Subjects (OPRS) has announced new
training opportunities for 2006.
Starting in July, 2006, Don Workman, the Executive Director
of OPRS, will conduct monthly one-hour brown bag seminars on the
Registration
Registration is required. To register, please complete the registration form
and forward it to Edwina Palacios via e-mail at:
e-palacios@northwestern.edu
or fax: 312-503-0555.
Schedule:
| |
|||
|
Topic |
Seminar
Content |
Date,
Time & Location |
Registration Deadline |
|
The Informed Consent Process |
Federal
requirements Consent
form document Alteration
of the consent Non-English
speaking Subjects |
Tuesday, July 25 Location: McGaw 1-401 |
July
18 |
|
Genetic Research and genetic testing: Risks and IRB requirements |
Special
considerations in protocols and consent forms Risks
& benefits Identifiers
& confidentiality Data
and tissue storage |
Tuesday, August 22 Location: Searle Seminar Room |
August
15 |
|
How to write an effective consent or assent document |
Required
elements 45CFR46.1116 NU
consent form template and guidelines Lay
language |
Friday, September 29 Location: To
be announced. |
September
22 |
|
HIPAA for Research: A Refresher |
HIPAA
Authorization combined with Consent form? Waiver
of Authorization Review
for preparatory for research Research
on decedents information Revision
of NU-HIPAA policy and its impact on the recruitment of subjects Limited
data set |
Thursday, October 26 Location: McGaw 1-401 |
October
19 |
|
Minimizing Risk of Harm and Reducing Regulatory Burden in Human Subjects Research |
When
research does not meet the definition of “human subjects research” Exempt
research Waivers
of consent and documentation |
November
To
be announced. |
|
|
IRB Member Initial Training |
What
we require Panel Members to know |
December To
be announced |
|
| |
|||
|
Topic |
Seminar
Content |
Date,
Time & Location |
Registration Deadline |
|
The Informed Consent Process |
Federal
requirements Consent/Assent
documents Waivers
and Alteration of consent Non-English
speaking Subjects |
Friday, July 7 Location: Tech LR5
|
July
3 |
|
Research using students as subjects: Risks and IRB requirements |
Special
considerations in protocols and consent forms Alternatives
to participation Parental
Permission Handling
Complaints |
Wed., August 9 Location: CHH |
August
2 |
|
How to write an effective consent or assent document |
Required
elements 45CFR46.116 NU
consent form template and guidelines Lay
language |
Friday, Sept. 8 Location: CHH |
September
1 |
|
Student research projects: What regulatory oversight is needed? |
When
are these projects human subjects research? When
do they qualify for exemption? What
ethical guidelines should be applied? How
do you handle subject complaints? |
Wed., October 11 Location:
To be announced. |
October
4 |
|
Minimizing Risk of Harm and Reducing Regulatory Burden in Human Subjects Research |
When
research does not meet the definition of “human subjects research” Exempt
research Waivers
of consent, and documentation |
Friday, November 10 Location: CHH |
November
3 |
|
IRB Member Initial Training: |
What
we require Panel Members to know |
TBA Location:
To be announced. |
|
For additional information, please
visit the OPRS web site:
Please contact Laurence Butaud-Rebbaa with questions:
- 312.503.3259 or l-butaud@northwestern.edu
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