The text of any Federal regulation cited in these policies may be found using the Electronic Code of Federal Regulations (e-CFR).
The text of any California law cited in these policies may be found using the Official California Legislative Information website.
The IRB/OHRPP Policy Compilation (a 3 Mb searchable PDF file) includes all the individual policies listed below. - Temporarily Unavailable
| 1 |
UCLA Policy 991: Protection of Human Subjects in Research |
January 23, 2009 |
| 2 |
Determining Which Research Activities Require UCLA OHRPP/IRB Review |
January 27, 2009 |
| 4 |
Research Conducted by UCLA Students |
February 26, 2009 |
| 5 |
OPRS Review Process - Certification of Exemption from IRB Review |
February 26, 2009 |
| 6 |
IRB Review Process - Initial Review |
February 26, 2009 |
| 7 |
Materials Required for IRB Review |
April 14, 2009 |
| 8 |
IRB Review Process - Expedited Review |
March 5, 2009 |
| 9 |
IRB Review Process - Full Committee Review |
July 5, 2007 |
| 10 |
IRB Review Process - Continuing Review |
February 26, 2009 |
| 11 |
IRB Review of Modifications to Previously Approved Research |
July 5, 2007 |
| 12 |
IRB Review Process - Communication of IRB Actions |
February 26, 2009 |
| 13 |
Referral to the IRB Executive Committee |
February 26, 2009 |
| 15 |
Biomedical Adverse Event Reporting
Please refer to HRPP Guidance &
Procedure 57 |
|
| 16 |
IRB Process - Consultant Review |
July 5, 2007 |
| 17 |
Closure of Human Subjects Research Studies |
April 27, 2009 |
| 18 |
Approvals From Other UCLA and External Committees |
February 26, 2009 |
| 20 |
Special Considerations for Projects Involving Vulnerable Populations |
February 26, 2009 |
| 21 |
Special Subject Populations: Children |
February 26, 2009 |
| 22 |
Special Subject Populations: Pregnant Women, Human Fetuses, and Neonates |
July 5, 2007 |
| 23 |
Special Subject Populations: Prisoners |
July 5, 2007 |
| 24 |
Special Subject Populations: Cognitively Impaired |
July 5, 2007 |
| 25 |
Special Subject Populations: Students and Employees |
March 5, 2009 |
| 26 |
Special Subject Populations: Non-English Speaking Subjects |
March 6, 2009 |
| 27 |
Third Party Subjects (a.k.a., Secondary Subjects) |
July 5, 2007 |
| 28 |
Subject Pools and Recruitment Databases |
March 6, 2009 |
| 29 |
Informed Consent Process and Documentation |
February 26, 2009 |
| 29a |
The Use of Legally Authorized Representatives or Surrogate Consent |
February 26, 2009 |
| 30 |
Recruitment Methods & Tools |
July 5, 2007 |
| 31 |
Payment for Participation in Research |
July 5, 2007 |
| 32 |
Financial Obligations |
July 5, 2007 |
| 33 |
Emergency Care and Compensation for Injury |
July 5, 2007 |
| 34 |
FDA Requirements |
February 11, 2008 |
| 35 |
IRB Approved Research in an Emergency Setting |
February 11, 2008 |
| 36 |
Emergency Use of a Test Article |
May 14, 2009 |
| 37 |
Genetics Research |
April 14, 2009 |
| 38 |
Human Embryonic Stem Cell Research |
July 5, 2007 |
| 39 |
Research Collection, Use, and Secondary Analysis of Human Specimens and/or Data |
April 13, 2009 |
| 40 |
Data and Specimen Repositories |
April 13, 2009 |
| 41 |
Data Safety Monitoring Plan |
April 10, 2009 |
| 42 |
Research Involving Public Use Data Files |
March 5, 2009 |
| 43 |
Data Security in Research |
April 8, 2009 |
| 44 |
Research Involving the Internet |
July 5, 2007 |
| 45 |
Research Involving Multiple Performance Sites or Collaborating Agencies or Institutions |
February 11, 2008 |
| 46 |
Research Conducted in International Settings |
July 5, 2007 |
| 47 |
Family Educational Rights and Privacy Act (FERPA) |
July 5, 2007 |
| 48 |
Protection of Pupil Rights Amendment (PPRA) |
July 5, 2007 |
| 49 |
Health Insurance Portability and Accountability Act (HIPAA) |
July 5, 2007 |
| 51 |
Reporting Suspected Abuse of Children, Elderly Individuals, and Others |
July 5, 2007 |
| 52 |
Reporting of Diseases and Conditions Identified in the Course of Research |
July 5, 2007 |
| 53 |
Noncompliance and Allegations of Noncompliance Regarding the Conduct of Human Subjects Research |
January 27, 2009 |
| 54 |
Consent Monitoring |
July 5, 2007 |
| 55 |
On Site Reviews of Human Research Studies |
November 12, 2009 |
| 56 |
HRPP Quality Improvement Activities |
April 14, 2009 |
| 57 |
Post-Approval Reporting Requirements for Investigators: Reporting of Unanticipated Problems, Including Adverse Events as well as Protocol Violations, Deviations and Incidents and the Reporting of Updated Study Safety Information |
May 13, 2009 |
| 58 |
Complaints and Concerns Regarding the Conduct of Human Subjects Research |
February 26, 2009 |
| 59 |
Suspension and Termination of Research |
February 26, 2009 |
| 60 |
Reporting Procedures For Unanticipated Problems, Noncompliance, Suspension, or Termination |
February 26, 2009 |
| 61 |
Investigator Responsibilities |
April 7, 2009 |
| 63 |
Investigator Financial Interests and Conflicts of Interest |
July 5, 2007 |
| 64 |
HRPP Education
and Training |
April 7, 2009 |
| 65 |
IRB Membership |
March 6, 2009 |
| 67 |
IRB Member Conflict of Interest |
July 5, 2007 |
| 69 |
IRB Meeting and Minutes |
February 26, 2009 |
| 70 |
IRB Office Records |
February 26, 2009 |
| 71 |
Media Interviews |
July 5, 2007 |
| Human Embryonic Stem Cell Research and IRB Review |
Jan 05, 2007 |
|
Certificate of Confidentiality |
August 4, 2008 |
|
Disclosure of Possible Conflict of Interest to Human Research Subjects |
April 20, 1999 |
|
Emergency Care and Compensation for Injury |
March 16, 2006 |
|
Fees for Reviews of Industry-Sponsored Clinical Trials |
2002 |
|
Gift Policy and Human Subjects Research |
April 6, 2004 |
|
HIPAA |
May 2005 |
|
HIV Reporting |
July 6, 2006 |
|
Navy-Supported Research |
June 6, 2007 |
|
Oral History |
December 10, 2003 |
|
Screening Research Subjects |
October 7, 2001 |
|
Suicide Risk and Research Protocols |
May 26, 2006 |
|
UCLA/RAND Memorandum of Understanding |
August 29, 2006 |
|
