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Keyword: Human Subjects
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List of Documents from Keyword Lookup
Guideline on Federal and UAB Requirements for the Protection of Human Research Participants: Ethical and Legal Framework for Human Research Protections at UAB - IRB POL002
Policy on the Protection of Human Subjects in Research
Procedure for Additional Safeguards for Children Involved in Research Including Assent - IRB PRO108
Procedure for Approving a Waiver or Alteration of the Consent Process and the Waiver of Consent Documentation - IRB PRO153
Procedure for Assurance of Compliance with Department of Health and Human Services Policy on Protection of Human Subjects - IRB PRO107
Procedure for Communicating Among IRBs - IRB PRO118
Procedure for Complaints and Inquiries for Research Participants, Investigators, Research Staff, and the Community - IRB PRO111
Procedure for Compliance Issues with Human Subjects Regulations or IRB Requirements or Determinations - IRB PRO128
Procedure for Conducting and Evaluating Activities Designed to Educate the Public about Human Subjects Research - IRB PRO130
Procedure for Confidentiality of Data; HIPAA Authorization and Waiver - IRB PRO112
Procedure for Continuing Review of Research Approved by the Convened IRB - IRB PRO147
Procedure for Continuing Review of Research by the Expedited Procedure - IRB PRO150
Procedure for Data and Safety Monitoring for Human Subjects Research - IRB PRO116
Procedure for Determination of Exemption from Human Subjects - IRB PRO105
Procedure for Determination that Necessary Resources are Available for Care and Safety of Human Research Participants - IRB PRO137
Procedure for Determination that Research Risks to Subjects Are Minimized - IRB PRO127
Procedure for Documentation of Convened IRB Proceedings - IRB PRO146
Procedure for Documentation of Research Undergoing Initial or Continuing Review by the Expedited Procedure - IRB PRO136
Procedure for Emergency Use of FDA-Regulated Test Articles - IRB PRO151
Procedure for Ensuring Qualifications of Investigators - IRB PRO103
Procedure for Evaluating and Training Individuals Involved in the Human Research Protection Program - IRB PRO100
Procedure for Facilitated Review of Industry-Sponsored Research by Western IRB (WIRB) - IRB PRO154
Procedure for Facilitated Review of Research for NCI Pediatric Central IRB-Approved Research Protocols - IRB PRO149
Procedure for Formation and Assignment of IRB Member Primary Review Teams for Initial or Continuing Review or Review of Modifications to Research at Convened IRB Meetings - IRB PRO144
Procedure for Identification and Communication of Human Subjects Research to Non-UAB-Affiliated Performance Sites - IRB PRO124
Procedure for Identification and Communication of Human Subjects Research to UAB-Affiliated Performance Sites - IRB PRO152
Procedure for Identifying and Managing Investigator and Institutional Conflicts of Interest - IRB PRO123
Procedure for Identifying and Managing IRB Member and Consultant Conflicting Interest - IRB PRO109
Procedure for Initial Review of Proposed Research at the Convened IRB Meetings - IRB PRO122
Procedure for Initial Review Using the Expedited Procedure - IRB PRO120
Procedure for IRB Meeting Agenda Development - IRB PRO142
Procedure for IRB Member Roster and Quorum - IRB PRO101
Procedure for IRB Member Selection for Convened Meeting - IRB PRO143
Procedure for IRB Use of Consultants - IRB PRO114
Procedure for Maintenance of IRB Records - IRB PRO126
Procedure for Not Human Subjects Research Designation - IRB PRO117
Procedure for Observation of the Informed Consent Process in Ongoing Research - IRB PRO129
Procedure for Organization of Protocol Files - IRB PRO115
Procedure for Participants to Communicate Questions and Concerns to Investigators and the IRB as Part of Informed Consent Process - IRB PRO131
Procedure for Policy Development and Communication for the Human Research Protection Program - IRB PRO110
Procedure for Qualifications and Composition of IRBs and OIRB - PRO104
Procedure for Quality Assurance (Monitoring of Human Subjects Research) - IRB PRO102
Procedure for Quality Assurance and Quality Improvement for the Human Research Protection Program - IRB PRO134
Procedure for Repositories of Human Tissues and Databanks - IRB PRO135
Procedure for Request for Documentation Regarding Use of Established Human Cell Lines Not Requiring IRB Review - PRO157
Procedure for Review of Decisionally Impaired Adults Involved in Human Subjects Research Including Assent - IRB PRO125
Procedure for Review of Modifications to Previously Approved Research by the Convened IRB - IRB PRO148
Procedure for Review when Pregnant Women, Fetuses, and Neonates are Involved as Participants in Research - IRB PRO132
Procedure for Review when Prisoners are Involved as Participants - IRB PRO133
Procedure for Reviewing and Signing of Independent Investigator Agreements - IRB PRO156
Procedure for Scientific/Scholarly Review of Protocols - IRB PRO138
Procedure for Selection and Recruitment of Subjects in Research - IRB PRO139
Procedure for Suspension or Termination of IRB-Approved Research and Administrative Hold - IRB PRO140
Procedure for the Informed Consent Process and Documentation of Informed Consent - IRB PRO113
Procedure for Timing of Document Distribution for Meetings - IRB PRO145
Procedure for Waiver to Informed Consent Process in Research Planned for Emergency Settings - IRB PRO119
Procedure on Maintaining the Privacy of Research Subjects - IRB PRO155
Procedure to Ensure Handling of Investigational or Unlicensed Test Articles Meets Organizational Standards Relating to Devices, Inventory Control and Documentation - IRB PRO141
Procedure to Ensure Prompt Reporting Of Unanticipated Problems Involving Risks to Subjects or Others to the IRB - IRB PRO106
Procedures to Ensure Handling of Investigational or Unlicensed Test Articles Meets Organizational Standards Relating to Pharmacy, Inventory Control, and Documentation - IRB PRO121
Roles and Responsibilities of the Institutional Review Board (IRB) - IRB POL004
UAB Expectations for Research Sponsors - IRB POL005
UAB Policy for Educational Activities on Human Research Protections for Participants, Prospective Participants, and the Community - IRB POL030
UAB Policy on Additional Safeguards for Children Involved in Research - IRB POL008
UAB Policy on Additional Safeguards for Pregnant Women and Fetuses and Neonates Involved in Research - IRB POL032
UAB Policy on Additional Safeguards for Prisoners Involved in Research - IRB POL033
UAB Policy on Additional Safeguards for Students Involved in Research - IRB POL041
UAB Policy on Assurance of Compliance with Department of Health and Human Services Policy on Protection of Human Subjects - IRB POL007
UAB Policy on Case Reports - IRB POL043
UAB Policy on Complaints and Inquiries for Research Participants, Investigators, Research Staff, and the Community - IRB POL011
UAB Policy on Compliance with Human Subjects Regulations or the Requirements of the IRB - IRB POL028
UAB Policy on Confidentiality of Data - IRB POL012
UAB Policy on Conflicts of Interest - IRB POL023
UAB Policy on Data Safety Monitoring for Human Subjects Research - IRB POL016
UAB Policy on Definition of "Legally Authorized Representative" for Decisionally Impaired Adults - IRB POL025
UAB Policy on Definition of Child, Parent, Guardian - IRB POL015
UAB Policy on Determination of Human Subject Research and Research Exempt from Federal Human Subjects Protection Regulations; IRB Review of Exempt Research - IRB POL017
UAB Policy on Determination of Human Subject Research on Cell Lines - IRB POL042
UAB Policy on Elements of Informed Consent, the Informed Consent Process, and Documentation of Informed Consent - IRB POL013
UAB Policy on Expedited Review of Human Subjects Research - IRB POL020
UAB Policy on Identification and Communication of Human Subjects - IRB POL029
UAB Policy on Inclusion of a Procedure for Participants to Communicate Questions and Concerns to Investigators and the IRB as Part of Informed Consent Process - IRB POL031
UAB Policy on IRB Consultants - IRB POL014
UAB Policy on IRB Member and Consultant Conflicting Interest - IRB POL009
UAB Policy on IRB Review of Human Subjects Research by Convened IRB - IRB POL022
UAB Policy on Maintaining the Privacy of Research Subjects - IRB POL037
UAB Policy on Maintenance of IRB Records - IRB POL026
UAB Policy on Minimizing Risks to Subjects - IRB POL027
UAB Policy on Other Laws Affecting Human Subjects Research - IRB POL040
UAB Policy on Policy Development and Communication for the Human Research Protection Program - IRB POL010
UAB Policy on Quality Assurance and Quality Improvement for the Human Research Protection Program - IRB POL034
UAB Policy on Reporting to Institutional Officials and Regulatory Agencies- IRB POL024
UAB Policy on Repositories of Human Tissue and Databanks - IRB POL035
UAB Policy on Scientific/Scholarly Review of Protocols - IRB POL003
UAB Policy on Selection and Recruitment of Subjects in Research - IRB POL039
UAB Policy on Suspension or Termination of IRB-Approved Research and Administrative Hold - IRB POL038
UAB Policy on the Establishment, Maintenance, and Utilization of IRBs - IRB POL018
UAB Policy on the Protection of Human Subjects in Research - IRB POL001
UAB Policy on Use of and Investigation with Drugs, Biologics, Devices, or Test Articles under FDA Regulations - IRB POL021
UAB Policy on Waiver of Informed Consent Requirements in Research Planned for Emergency Settings - IRB POL019
UAB Policy on Waiver, Alterations, and Exceptions to Informed Consent; Waiver of Documentation of Informed Consent - IRB POL036
UAB Policy to Ensure Prompt Reporting of Unanticipated Problems Involving Risks to Subjects or Others to the IRB - IRB POL006
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