Keyword Lookup Results

Keyword: Human Subjects

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