OHRP: IRB Records, Part Two
Sign in to YouTube
Sign in to YouTube
Sign in to YouTube
Uploaded on Sep 21, 2010
In this Office for Human Research Protections (OHRP) video, all of the characters are fictional. This video provides information regarding the IRB records requirements described at 45 CFR part 46. The institution portrayed in the video hired a consultant to evaluate its human subjects protections program. The consultant made a number of observations and findings regarding the institution's compliance with the requirements of the regulations.
In this video a consultant, Ms. Williams, meets with Mr. Cash, the new Director of the institution's IRB office, to review in detail the deficiencies she observed and requirements related to the IRB meeting minutes and other IRB records.
OHRP Educational Videos-Additional Information
OHRP educational videos were developed by the OHRP Division of Education and Development and are intended to provide information regarding the requirements of the Department of Health and Human Services (HHS) regulations for the protection of human subjects at 45 CFR part 46. The videos represent OHRP's current thinking on these topics and should be viewed as recommendations unless specific regulatory requirements are cited. The use of the word must in OHRP guidance means that something is required under HHS regulations at 45 CFR part 46. The use of the word should in OHRP guidance means that something is recommended or suggested, but not required. An institution may use an alternative approach if the approach satisfies the requirements of the HHS regulations at 45 CFR part 46. OHRP is available to discuss alternative approaches at 240-453-6900 or 866-447-4777.
More more information, please visit: http://www.hhs.gov/ohrp
From the U.S. Department of Health and Human Services (HHS) http://www.hhs.gov
-
Category
-
License
Standard YouTube License
Loading...
Loading...
Loading...
Loading...
Loading...
Next in Office for Human Research Protections (OHRP)
Suggestions
-
6:59
TRIOby Stephen MatthewsFeatured
1,040
-
25:18
OHRP: Reviewing and Reporting Unanticipated Problems and Adverse Eventsby USGOVHHS
6,369 views
-
28:13
OHRP: Research Involving Vulnerable Populationsby USGOVHHS
7,583 views
-
16:05
OHRP: IRB Membershipby USGOVHHS
8,155 views
-
3:21
PI at the IRBby schmedgar
4,270 views
-
1:55
GCP Training - Core Human Subject Protection Trailerby CambridgeHealthtech
1,087 views
-
1:22:40
Whose data is it anyway? Medical databases, privacy and trustby battleofideas
803 views
-
6:08
IRB Video #2 Types of Reviewby edutubechannel
134 views
-
4:30
IRB Video #1 Introby edutubechannel
421 views
-
18:39
OHRP: General Informed Consent Requirementsby USGOVHHS
8,527 views
-
7:53
Research ethics for undergraduate students.by UWNSHSS
4,094 views
-
5:08
Charlie on the IRBby PublicResponsibility
763 views
-
22:43
OHRP: Research Use of Human Biological Specimens and Other Private Informationby USGOVHHS
8,860 views
-
5:36
How do I work with the IRB?by RegisUniversity
1,671 views
-
1:58
Informed Consent Content and Process Requirements Trailerby CambridgeHealthtech
631 views
-
8:43:13
YYCCC 2011-03-07 Calgary City Council - Video Archive - March 7, 2011 - Secondary Suitesby gordonmcdowell
49,464 views
-
1:00:37
Desmystifying the IRBby geneticalliance
853 views
-
6:18
FDA 21 CFR Part 11 Integration in LabImage Platformby kapelanbioimaging
912 views
-
4:56
UT Undergraduate Researchby utsenate
3,005 views
-
7:32
On the Edge #8, 1 of 6: Ethics in lab & clinical researchby Dr. Jonas Moses
681 views
- Loading more suggestions...
All Comments