Name | Number Pages |
---|
IRB | 42 |
Research | 31 |
Top | 27 |
Institutional Review Board | 22 |
Food | 21 |
Drug Administration | 21 |
IRB Office | 20 |
Office | 20 |
FDA | 20 |
UIUC | 17 |
University of Illinois | 17 |
Human Services | 16 |
RPI | 15 |
IRBs | 15 |
IRB approval | 14 |
Belmont Report | 14 |
Sec | 13 |
Vice Chancellor | 13 |
Children | 12 |
Investigators | 12 |
Note | 12 |
Department of Health | 12 |
Information | 12 |
UIUC IRB | 11 |
IRB review | 11 |
Urbana Champaign | 11 |
Subjects | 11 |
HHS | 11 |
Federal Register | 11 |
OHRP | 10 |
Protection of Human Subjects | 10 |
Code of Federal | 10 |
Top Sec | 10 |
Risks | 9 |
IRB application | 9 |
State | 9 |
DHHS | 9 |
Human Research Protections | 9 |
Oct. 2 | 9 |
Responsible Project Investigator | 9 |
Data | 9 |
IRB members | 9 |
Examples | 8 |
IND | 8 |
Federal | 8 |
Common Rule | 8 |
UIUC policies | 8 |
NIH | 8 |
Informed Consent | 8 |
Chapter 6 | 7 |
Policy | 7 |
Click | 7 |
UIUC Institutional Review Board | 7 |
Institution | 7 |
Center | 7 |
HHS regulations | 7 |
United States | 7 |
Public Health Service Act | 7 |
IRB Web site | 7 |
UIUC Handbook | 6 |
Environmental Protection Agency | 6 |
Secretary | 6 |
Drugs | 6 |
IRB purposes | 6 |
Additional information | 6 |
Assent | 6 |
Director | 6 |
Title 45 | 6 |
Minimal risk | 6 |
Adobe Acrobat Reader | 6 |
Web site | 6 |
IDE | 6 |
Secretary of HHS | 6 |
MS Word | 6 |
Part 46 | 6 |
IND. | 6 |
D | 6 |
Mar. 4 | 6 |
Consent forms | 6 |
Applicability | 6 |
National Institutes of Health | 6 |
Acrobat Reader | 6 |
Date | 5 |
Institutions | 5 |
Commissioner | 5 |
Handbook | 5 |
Inspection Service | 5 |
Federal Food | 5 |
Human Subjects | 5 |
UIUC faculty | 5 |
B | 5 |
UIUC IRB Office | 5 |
FDA regulations | 5 |
Compliance | 5 |
Mar. 19 | 5 |
Act | 5 |
IRB meetings | 5 |
Applications | 5 |
Records | 5 |
Contents | 5 |
Use | 5 |
Introduction | 5 |
Research Risks | 5 |
UIUC Federalwide Assurance | 5 |
Institutional Review Boards | 5 |
June 17 | 5 |
Board | 5 |
Documentation | 5 |
Participation | 5 |
MRI | 5 |
Health | 5 |
Human subject | 5 |
Food Safety | 5 |
Department | 5 |
Contracts | 5 |
IRB meeting | 5 |
Fetuses | 5 |
IRB approval of research | 5 |
Section | 5 |
OHRP Guidebook Research | 5 |
Research Subject | 5 |
Investigator | 5 |
Biomedical | 5 |
Cosmetic Act | 5 |
Approval | 5 |
Drug | 5 |
Protection | 5 |
Jan. 27 | 5 |
Subject | 5 |
UIUC employee | 5 |
Students | 4 |
Notice | 4 |
Title 45 Code of Federal | 4 |
FDA approval | 4 |
DHHS regulations | 4 |
Biologics Evaluation | 4 |
Dockets Management Branch | 4 |
Docket Number | 4 |
Behavioral Research | 4 |
Access | 4 |
Sponsor | 4 |
Devices | 4 |
Inclusion | 4 |
Secretary of Health | 4 |
Benefits | 4 |
Rockville | 4 |
Drug Evaluation | 4 |
Exemptions | 4 |
OPRR | 4 |
Application | 4 |
UIUC Investigator Handbook | 4 |
IRB member | 4 |
Chair | 4 |
Jan. 5 | 4 |
Individuals | 4 |
Human Subjects Research | 4 |
Form | 4 |
Sept. 5 | 4 |
Guidelines | 4 |
Studies | 4 |
Federal Policy | 4 |
Subpart A | 4 |
Assurance | 4 |
Persons | 4 |
UIUC department | 4 |
Essential Elements | 4 |
Definitions | 4 |
May | 4 |
UIUC researchers | 4 |
MD 20857 | 4 |
CT | 4 |
Copies | 4 |
Mar. 29 | 4 |
Pregnant Women | 4 |
Women | 4 |
General | 4 |
Top Placeholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder text textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder textPlaceholder | 4 |
Informed consent | 4 |
Secs | 4 |
Researchers | 4 |
II | 4 |
Declaration of Helsinki | 4 |
Review | 4 |
Freedom of Information Act | 4 |
World Wide Web | 3 |
Questions | 3 |
Federal Government | 3 |
Clinical investigation | 3 |
President | 3 |
Interaction | 3 |
Intervention | 3 |
Nov. 5 | 3 |
University | 3 |
Appendix A | 3 |
US Department of Agriculture | 3 |
January 2003 Approved | 3 |
IRB reviews | 3 |
NOTE | 3 |
Chancellor | 3 |
UIUC IRB. | 3 |
UIUC students | 3 |
Adverse Events | 3 |
Authorization | 3 |
Statements | 3 |
Research Equipment Form | 3 |
IRB information | 3 |
Anonymity | 3 |
Jan. 18 | 3 |
Subpart D | 3 |
Private information | 3 |
Illinois | 3 |
Agents | 3 |
Dec. 2 | 3 |
Nonviable neonates | 3 |
Devices Form | 3 |
IRB Chair | 3 |
Exemption 2 | 3 |
Phase 2 | 3 |
Criteria | 3 |
Others | 3 |
Adequate provision | 3 |
C | 3 |
Viable neonates | 3 |
More | 3 |
IRB committee | 3 |
Such | 3 |
See | 3 |
Category | 3 |
Protocol Amendment | 3 |
Washington | 3 |
Phase 3 studies | 3 |
Changes | 3 |
Identification | 3 |
Questionnaires | 3 |
Nuremberg Code | 3 |
Protocols | 3 |
Cases | 3 |
UIUC policy | 3 |
October 1 | 3 |
Exemption 5 | 3 |
Explicit consent | 3 |
Appendix B | 3 |
Word | 3 |
American Anthropological Association | 3 |
Approved cases | 3 |
Exemption 5 cannot | 3 |
Pilot projects | 3 |
HHS guidelines | 3 |
U.S. | 3 |
Investigational Device Exemption | 3 |
Minor modifications | 3 |
Research Academic Policies | 3 |
Federal regulations | 3 |
IRB membership | 3 |
Research Amendment form | 3 |
Source | 3 |
May 22 | 3 |
Top 3 | 3 |
Mere failure | 3 |
Nothing | 3 |
Protocol | 3 |
Confidentiality | 3 |
Expedited Review | 3 |
More information | 3 |
Vital functions | 3 |
Consent | 3 |
Federalwide Assurance | 3 |
American Sociological Association | 3 |
Bethesda | 3 |
June 18 | 3 |
References | 3 |
Anyone responsible | 3 |
UIUC IRBs | 3 |
Consent Process | 3 |
Detailed guidelines | 3 |
Minimal Risk | 3 |
Education | 3 |
Participants | 3 |
Oct. 20 | 3 |
Neonates | 3 |
English | 3 |
IRB Review | 3 |
State of Illinois | 3 |