Institutional Review Board

Human Participants (IRB)
Animal Subjects (IACUC)
Conflict of Interest
Scientific Misconduct
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Participant Outreach
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TOPICAL LIST OF UA IRB POLICIES, FORMS, AND GUIDANCE DOCUMENTS

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TOPIC


POLICY/PROCEDURE


FORMS


GUIDANCE

Adverse Events

Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF

Report of Study Problem

Word    PDF

Reportable Events

Word    PDF

Advertising/
Recruitment

Subject Recruitment and Compensation

Word    PDF

 

IRB Advertising Guidelines

Word    PDF

Alabama Law

 

 

Alabama Law on Children,  Minors, Consent, and Other Research-Related Topics  

Word    PDF


Mandatory Reporting Laws Affecting Research Conducted in Alabama

Word    PDF

Assent

Protection of Children In Research

Word    PDF


Protection of the Cognitively Impaired

Word    PDF

Application for Research Involving Children

Word    PDF


Application for Research with Cognitively Impaired Persons

Word    PDF

A Pediatric Research “Assent Matrix”

Word    PDF


Examples of Assent Forms

Word    PDF


Alabama Law on Children,  Minors, Consent, and Other Research-Related Topics  

Word    PDF

Assessing Participant Comprehension

Investigator Assessment of Participant Comprehension

Word    PDF

Decision-Making Capacity Assessment Tool

Word    PDF

 

Assurance of Compliance

Terms of UA Federalwide Assurance

Word    PDF

   

Authority of IRB

 

Human Research Participant Protection Plan

Word    PDF


Authority and Independence of the IRB in Protecting Human Research Participants  

Word    PDF


Institutional Commitment to the Protection of Human Subjects by the IRB

Word    PDF

 

 

Case/Chart/Record Review

Research Utilizing Records, Chart Reviews, and Case Studies/Reports  

Word    PDF

 

Children/Minors

Protection of Children In Research

Word    PDF

Application for Research Involving Children

Word    PDF

Alabama Law on Children,  Minors, Consent, and Other Research-Related Topics  

Word    PDF


A Pediatric Research “Assent Matrix”

Word    PDF


Examples of Assent Forms

Word    PDF


Family Educational Rights and Privacy Act (FERPA)

Word    PDF


Legislation on School-Based Surveys and Passive Consent:  No Child Left Behind

Word    PDF


Investigators and Legally Authorized Representatives

Word    PDF

Closure of Studies

Closure of IRB Protocols

Word    PDF

Request for Study Closure

Word PDF

Cognitively Impaired Persons

Protection of the Cognitively Impaired

Word    PDF


Investigator Assessment of Participant Comprehension

Word    PDF

Application for Research with Cognitively Impaired Persons

Word    PDF


Decision-Making Capacity Assessment Tool

Word    PDF

Investigators and Legally Authorized Representatives

Word    PDF

Community-Based, Participatory Research

 

IRB Checklist for Reviewers and Investigators

Word    PDF

 

Community Education

Educational Opportunities for the Community

Word    PDF

 

 

Complaints and Concerns

Investigator and Staff Responses to Participants’ Questions, Complaints, and Concerns   

Word    PDF


Participant and Community Questions, Suggestions, Complaints, and Concerns About Research Studies

Word    PDF


Allegations and Findings of Noncompliance

Word    PDF


Monitoring of Previously Approved Research for Cause:  Suspension and Termination

Word    PDF


Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF

Question or Suggestion for IRB

Word    PDF


Report of Complaint or Concern About Research Study

Word    PDF


Survey for Participants in UA Sponsored Research Study

Word    PDF


Research Staff Satisfaction with Study

Word    PDF

Reportable Events

Word    PDF


General Responsibilities of Investigators

Word    PDF


Template: Informed Consent for a Medical or Health-Related Study

Word    PDF


Template:  Informed Consent for a Non-Medical Study

Word    PDF

Conduct of IRB Meetings

 

 

 

 

 

Full Board Review of Protocols

Word    PDF


Documentation of IRB Discussions and Decisions (IRB Minutes)

Word    PDF


IRB Record Keeping and Management

Word    PDF

IRB Members’ Pledge of Confidentiality of IRB Deliberations and Protocol Content

Word    PDF

 

Confidentiality of Participants/Organizations

 

 

Protection of Human Research Participants’ Privacy and Confidentiality

Word    PDF


Research Using a Restricted Access Data Set

Word    PDF


Research Using a Limited Data Set

Word    PDF

IRB Checklist for Reviewers and Investigators

Word    PDF


Authorization on Use or Disclosure of Health Information

Word    PDF


Request for Partial Waiver of Patient Authorization to use PHI for Recruitment or Screening

Word    PDF

IRB Application Guide

Word    PDF


Protection of Human Subjects in HIV/AIDS Related Research

Word    PDF


Template: Informed Consent for a Medical or Health-Related Study

Word    PDF


Template:  Informed Consent for a Non-Medical Study

Word    PDF

 Conflict of Interest-IRB

Conflict of Interest for IRB Members, Chairs, and Consultants

Word    PDF

IRB Member Disclosure of COI

Word    PDF

 

Conflict of Interest –PIs

IRB and Investigator Responsibilities for Applications Involving Declared or Undeclared Investigator Conflict of Interest

Word    PDF


UA Policy on Conflict of Interest/Financial Disclosure in Research and Other Sponsored Programs

PDF

Investigator Statement of Financial Interest

PDF

 

Conflict of Interest—Institutional

UA policy in progress

   

Consultation (for IRB)

Obtaining Additional Expertise or Expert Consultation for IRB Reviews

Word    PDF

Translator’s Declaration

Word    PDF

 

Continuing Review/Renewal

Continuing Review of Approved IRB Protocols

Word    PDF

IRB Renewal Application

Word    PDF


Log of Study Problems

Excel    PDF

 

Copyright Law

 

Copyrighted Instruments and IRB Applications

Word    PDF

Creation of Policies

Creation, Revision, Review, and Dissemination of Policies for the Human Research Protection Program

Word    PDF

   

Data Safety and Monitoring

 

 

 

Data and Safety Monitoring in Proposed Research

Word    PDF

 

 

        

IRB Checklist for Reviewers and Investigators

Word    PDF

Developing a Data and Safety Monitoring Plan (DSMP) or a Data And Safety Monitoring Board (DSMB)

Word    PDF


IRB Application Guide

Word    PDF

Data Sets

Review for Exemption

Word    PDF


Research Using Publicly Available Data Sets

Word    PDF


Research Using a Limited Data Set

Word    PDF


Research Using a Restricted Data Set

Word    PDF

 

Public Datasets Approved for Secondary Analysis Without IRB Review

Word    PDF


The Meaning of Anonymous, Confidential, and De-Identified and Implications for Data Sharing or Re-Use

Word    PDF

Deception/Concealment

Waivers, Alterations, and Exceptions to Informed Consent or its Written Documentation

Word    PDF

Request for Waiver/Alteration of Informed Consent

Word    PDF

Use of Deception/Concealment in Research

Word    PDF

Department of Defense Research

 

 

Department of Defense Regulations for Human Subjects Research

Word    PDF

Department of Energy Research
   

Department of Energy Regulations for Human Subjects Research

Word    PDF

Emergency Use of Test Article

Emergency Use of a Test Article

Word    PDF

Notification to IRB of Emergency Use of a Test Article

Word    PDF

 

Environmental Protection Agency Research

   

Environmental Protection Agency Requirements for Human Subjects Research

Word    PDF

Equitable Selection of Subjects

 

Appropriate and Equitable Selection of Subjects

Word    PDF

 

 

Exempt Research

Review for Exemption

Word    PDF


Research Using a Restricted Access Data Set

Word    PDF


Research Using a Limited Data Set

Word    PDF


Research Utilizing Records, Chart Reviews, and Case Studies/Reports

Word    PDF

Exemption Eligibility Checklist

Word    PDF

 

Expedited Review

 

Expedited Review

Word    PDF

   

Face Pages, IRB Application (Required)

 

 

Request for Approval of Research Involving Human Subjects (Page 1)

Word    PDF


IRB Application  Study Personnel  Sheet (Page 2)

Word    PDF


Signature Assurance Sheet (Page 3)

Word    PDF

 

Faculty 

Faculty Use of Students as Human Research Participants and Paid or Unpaid Assistants in Their Research

Word    PDF


University Expectations for Persons Involved with the Human Research Protections Program

Word    PDF

Certification of Responsibility of a Graduate Research Assistant or Graduate Teaching Assistant Employed on Grants, Contracts, and Other Sponsored Projects

Word    PDF


Signature Assurance Sheet

Word    PDF

IRB Application Guide

Word    PDF


Meaning of Departmental Signature on Signature Assurance Sheet

Word    PDF

FDA-regulated Research

Conformity of Investigational or Unlicensed Test Articles (Devices) to Federal Regulations

Word    PDF


Conformity of Investigational or Unlicensed Test Articles (Drugs, Biologics) to Federal Regulations

Word    PDF

 

Regulatory Requirements for Investigators Who Hold INDs or IDEs

Word    PDF

FERPA

 

 

Family Educational Rights and Privacy (FERPA)

Word    PDF

Fetuses & Neonates

Protection of Pregnant Women, Fetuses, & Neonates

Word    PDF

Application for Research Involving Pregnant Women, Human Fetuses, and/or Neonates

Word    PDF

 

Full Board Review

 

Full Board Review of Protocols

Word    PDF


Obtaining Additional Expertise or Expert Consultation for Full Board Reviews

Word    PDF

Completeness of IRB Application

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF

IRB Application Guide

Word    PDF

HIV/AIDS

 

 

Protection of Human Subjects in HIV/AIDS-Related Research

 Word    PDF

Human Research Determination

Human Research Determination

Word    PDF

Human Research Determination Checklist (DHHS & FDA)

Word    PDF

 

Human Subjects Training

University Expectations for Persons Involved with Human Research Protection Program

Word    PDF


Improving Qualifications and Expertise of IRB Members, Investigators, and Office for Research Staff

Word    PDF

 

See website for current training requirements

IND/IDE

Conformity of Investigational or Unlicensed Test Articles (Devices) to Federal Regulations

Word    PDF


Conformity of Investigational or Unlicensed Test Articles (Drugs, Biologics) to Federal Regulations

Word    PDF

 

Regulatory Requirements for Investigators Who Hold INDs or IDEs

Word    PDF

Independence of IRB

Human Research Protection Program Plan

Word    PDF


Institutional Commitment to Protection of Human Subjects by the IRB

Word    PDF

Report of Attempt to Exert Undue Influence

Word    PDF

 

Informed Consent

Investigator Responsibilities for Informed Consent Process and Documentation

Word    PDF


Investigator Assurance of Participation Comprehension

Word    PDF


Research Involving the Internet

Word    PDF


Protection of Children in Research

Word    PDF


Protection of the Cognitively Impaired  

Word    PDF


Research Involving Prisoners

Word    PDF


Waivers, Alterations, and Exceptions to Informed Consent or its Written Documentation

Word    PDF

IRB Checklist for Reviewers and Investigators

Word    PDF


Decision-Making Capacity Assessment Tool

Word    PDF


Observation of Consent Process

Word    PDF


Request for Waiver of Written Documentation of Informed Consent

Word    PDF


Request for Waiver/Alteration of Informed Consent

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF

Informed Consent  

Word    PDF


IRB Application Guide

Word    PDF


Writing Understandable Consent Forms  

Word    PDF


Template:  Informed Consent for a Medical or Health-Related Study  

Word    PDF


Sample Consent Form for a Medical /Health-Related Study

Word    PDF


Template:  Informed Consent for a Non-Medical Study

Word    PDF


Sample Consent Form for a Non-Medical Study

Word    PDF


Model Telephone Consent

Word    PDF


Template for Study Presentations for Web Surveys

Word    PDF


Use of Deception/Concealment in Research

Word    PDF


The Meaning of Anonymous, Confidential, and De-Identified and Implications for Data Sharing or Re-Use

Word    PDF


Investigators and Legally Authorized Representatives

Word    PDF

International Research

 

 

International Research

Word    PDF

Internet Research

Research Involving the Internet

Word    PDF

 

Template for Study Presentations for Web Surveys

Word    PDF

Investigator Input to IRB

Investigator Input into the HRPP/IRB Review Process

Word    PDF

Question/Suggestion for IRB/HRPP

Word    PDF

 

Investigator Responsibilities

 

 

 

 

University Expectations for Persons Involved with Human Research Protection Program

Word    PDF


Qualifications and Responsibilities of Investigators

Word    PDF


IRB and Investigator Responsibilities for Applications Involving Declared or Undeclared Investigator Conflict of Interest

Word    PDF


Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF


Investigator and Staff Response to Participants’ Questions, Complaints, and Concerns

Word    PDF


Investigator Responsibilities for Informed Consent Process and Documentation

Word    PDF


Investigator Assessment of Participant Comprehension

Word    PDF

PI Statement of Conflict of Interest

Electronic


Report of Study Problem

Word    PDF


Log of Study Problems

Excel    PDF


Decision-Making Capacity Assessment Tool

Word    PDF

General Responsibilities of Investigators

Word    PDF


Student Researchers at UA

Word    PDF


Reportable Events

Word    PDF


Informed Consent

Word    PDF


IRB Application Guide

Word    PDF


Template:  Informed Consent for a Medical or Health-Related Study

Word    PDF


Template:  Informed Consent for a Non-Medical Study

Word    PDF


Investigators and Legally Authorized Representatives

Word    PDF

 

IRB Application

 

Study Personnel & Study Responsibilities Page

Word    PDF


Completeness of IRB Applications

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF


Request for Approval Form (Page 1, IRB Application)

Word    PDF

IRB Application Guide

Word    PDF

IRB Determinations and Motions

 

 

IRB Determinations and Motions

Word    PDF

IRB Job Descriptions

 

Study Personnel & Study Responsibilities Page

Word    PDF


Completeness of IRB Applications

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF


Request for Approval Form (Page 1, IRB Application)

Word    PDF

 

Legal Age/Adulthood in Alabama

 

 

Alabama Law on Children, Minors, Consent, and Other Research-Related Topics

Word    PDF

Minor Changes

IRB Application for Modifying Approved Protocols

Word    PDF

Modification of an Approved Protocol

Word    PDF

Minor Changes to Approved Protocols

Word    PDF

Misconduct

Allegations and Findings of Noncompliance

Word    PDF


UA Policy on Misconduct is in revision

Report of Study Problem

Word    PDF

Reportable Events

Word    PDF

Modifying Approved Protocols

 

IRB Application for Modifying Approved Protocols

Word    PDF


Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF

Modification of an Approved Protocol

Word    PDF

Minor Changes to Approved Protocols

Word    PDF

 


Reportable Events

Word    PDF

 

Monitoring for Cause

Monitoring of Previously Approved Research for Cause:  Suspension and Termination

Word    PDF

Report of Study Problem

Word    PDF


Report of Complaint or Concern About a Research Study

Word    PDF

Reportable Events

Word    PDF

Multi-Site Research

Review and Oversight of Research Conducted at Multiple Sites

Word    PDF

 

 

No Child Left Behind

 

 

Legislation on School-Based Surveys and Passive Consent: No Child Left Behind

Word    PDF

Noncompliance

Allegations and Findings of Noncompliance

Word    PDF


Monitoring of Previously Approved Research for Cause:  Suspension and Termination

Word    PDF


Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF

Report of Study Problem

Word    PDF


Report of Complaint or Concern About a Research Study

Word    PDF

Reportable Events

Word    PDF

Oral History

 

 

Information on Oral History Projects

Word    PDF

Participant Outreach

Participant and Community Questions, Suggestions, Complaints, and Concerns About Research Studies

Word    PDF


Monitoring of Previously Approved Research for Cause: Suspension and Termination

Word    PDF

Report of Complaint or Concern About Research Study

Word    PDF


Question or Suggestion for IRB/HRPP

Word    PDF


Survey for participants in UA Sponsored Research Study

Word    PDF

Research and You:  Know Your Rights
(In English and Spanish)

Word    PDF


Template: Informed Consent for a  Medical or Health-Related Study

Word    PDF


Template: Informed Consent for Non-Medical Study

Word    PDF

Post Approval Monitoring

Routine Post Approval Monitoring of  Protocols (PAM)

Word    PDF

Checklist for Monitoring Approved Exempt Protocols

Word    PDF


Checklist for Post-Approval Monitoring of Expedited and Full Board Protocols (Long Form)  

Word    PDF


Observation of Consent Process

Word    PDF


Post Approval Monitoring Checklist (Short Form)

Word    PDF

 

Pregnant Women

Protection of Pregnant Women, Fetuses, & Neonates

Word    PDF

Application for Research Involving Pregnant Women, Human Fetuses, and/or Neonates

Word    PDF

 

Prisoners

Research Involving Prisoners

Word    PDF

Application for Research Involving Prisoners

Word    PDF

 

Privacy

Protection of Human Research Participants’ Privacy and Confidentiality

Word    PDF


Research Using a Restricted Access Data Set

Word    PDF


Research Using a Limited Data Set

Word    PDF


Research Utilizing Records, Chart Reviews, and Case Studies/Reports  

Word    PDF

IRB Checklist for Reviewers and Investigators

Word    PDF


Authorization of Use or Disclosure of Health Information

Word    PDF


Request for Partial Waiver of Patient Authorization to use PHI for Recruitment or Screening

Word    PDF

Protection of Human Subjects in HIV/AIDS-Related Research

Word    PDF


IRB Application Guide

Word    PDF


Template: Informed Consent for a  Medical or Health-Related  Study  

Word    PDF


Template: Informed Consent for Non-Medical Study

Word    PDF

Reportable Events

Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF

Report of Study Problem

Word    PDF


Log of Study Problems

Excel    PDF

Reportable Events

Word    PDF

Research by Students

Qualifications and Responsibilities of Investigators

Word    PDF


Improving Qualifications and Expertise for IRB Members, Investigators, and Office for Research Staff

Word    PDF


Investigator and Staff Response to Participants’ Questions, Complaints, and Concerns

Word    PDF

Signature Assurance Sheet

Word    PDF

General Responsibilities of Investigators

Word    PDF


Student Researchers at UA

Word    PDF


Meaning of Departmental Signature on the Signature Assurance Sheet

Word    PDF

Research-Related Injury

 

Sponsored Projects Agreements for Human Subjects Research and Human Research Protections

Word    PDF

 

Template: Informed Consent for a  Medical or Health-Related  Study

Word    PDF


Template: Informed Consent for Non-Medical Study

Word    PDF

Required Signatures

 

Signature Assurance Sheet

Word    PDF

Meaning of Departmental Signature on Signature Assurance Sheet

Word    PDF

Risk Identification & Management

 

Identifying and Minimizing Risks to Human Research Participants 

Word    PDF


Investigator Responsibilities for Informed Consent Process and Documentation

Word    PDF


Data and Safety Monitoring in Proposed Research

Word    PDF


IRB Application for Modifying Approved protocols

Word    PDF

IRB Checklist for Reviewers and Investigators

Word    PDF


Modification of an Approved Protocol

Word    PDF

Evaluating Sound Study Design

Word    PDF


IRB Application Guide

Word    PDF


Informed Consent

Word    PDF


Template:  Informed Consent for a Medical/Health Related Study

Word    PDF


Template: Informed Consent for Non-Medical Study

Word    PDF

Scientific/Scholarly Validity

 

IRB Checklist for Reviewers and Investigators

Word    PDF


Signature Assurance Sheet

Word    PDF

Evaluating Sound Study Design

Word    PDF


IRB Application Guide

Word    PDF


Meaning of Departmental Signature on the Signature Assurance Sheet

Word    PDF

Schools, School Children

Protection of Children in Research

Word    PDF

Application for Research Involving Children

Word    PDF

A Pediatric Research “Assent Matrix”

Word    PDF


Examples of Assent Forms

Word    PDF


Family Educational Rights and Privacy (FERPA)

Word    PDF


Legislation on School-Based Surveys and Passive Consent: No Child Left Behind

Word    PDF

Selecting Subjects

 

 

 

 

 

 

 

Appropriate and Equitable Selection of Subjects

Word    PDF


Faculty Use of Students as Human Research Participants and Paid or Unpaid Assistants in Their Research

Word    PDF


Student Research Pools

Word    PDF


Protection of Children in Research

Word    PDF


Protection of the Cognitively Impaired

Word    PDF


Protection of Pregnant Women, Fetuses, and Neonates

Word    PDF


Research Involving Prisoners

Word    PDF

IRB Checklist for Reviewers and Investigators

Word    PDF


Application for Research Involving Children

Word    PDF


Application for Research Involving Cognitively Impaired Persons

Word    PDF


Application for Research Involving Pregnant Women, Human Fetuses, and/or Neonates

Word    PDF


Application for Research Involving Prisoners

Word    PDF

IRB Application Guide

Word    PDF

 

Sponsored Projects Agreements

Sponsored Projects Agreements for Human Subjects Research and Human Research h Protections

Word    PDF

   

Student Investigators 

 

See also Investigator Responsibilities

 

 

Improving Qualifications and Expertise for IRB Members, Investigators, and Office for Research Staff

Word    PDF


Investigator and Staff Response to Participants’ Questions, Complaints, and Concerns

Word    PDF

 

 

 

Signature Assurance Sheet

Word    PDF

 

 

General Responsibilities of Investigators

Word    PDF


Student Researchers at UA

Word    PDF


Meaning of Departmental Signature on the Signature Assurance Sheet

Word    PDF

Student Research Participants

Faculty Use of Students as Human Research Participants and Paid or Unpaid Assistants in Their Research

Word    PDF


Student Research Pools

Word    PDF

Report of Complaint or Concern About Research Study

Word    PDF


Question or Suggestion for IRB

Word    PDF


Survey for Participants in UA-sponsored Research Study

Word    PDF 

Student Research Participants

Word    PDF

 

Student Research Pools

 

Student Research Pools

Word    PDF

Report of Complaint or Concern About Research Study

Word    PDF


Question or Suggestion for IRB

Word    PDF


Survey for Participants in UA-sponsored Research Study

Word    PDF

Student Research Participants

Word    PDF

Training And Supervision of  Research Staff

 

Certification of Responsibility for Graduate Research Assistant or Graduate Teaching Assistant Employed on Grants, Contracts, and Other Sponsored Projects

Word    PDF


Research Staff Satisfaction with Study Conduct

Word    PDF

General Responsibilities of  Investigators

Word    PDF


Reportable Events

Word    PDF

Telephone Research Consent

 

 

Model Telephone Consent

Word    PDF

UA Students

 

Student Research Pools

Word    PDF


Faculty Use of Students as Research Participants or Paid or Unpaid Assistants in their Research

Word    PDF

 

Report of Complaint or Concern About Research Study

Word    PDF


Question or Suggestion for IRB

Word    PDF


Survey for Participants in UA-sponsored Research Study

Word    PDF

Student Research Participants

Word    PDF


Student Researchers at UA

Word    PDF


Research and You:  Know Your Rights

Word    PDF

Unanticipated Problems

 

Reportable Events: Protocol Deviations, Unanticipated Problems, and Adverse Events

Word    PDF


IRB Application for Modifying Approved protocols

Word    PDF

Report of  Study Problem

Word    PDF


Modification of an Approved Protocol

Word    PDF


Log of Study Problems

Excel    PDF

Reportable Events

Word    PDF

Vulnerable Populations

 

Identifying and Minimizing Risks to Human Research Participants

Word    PDF


Protection of Children in Research

Word    PDF


Protection of the Cognitively Impaired

Word    PDF


Protection of Pregnant Women, Fetuses, and Neonates

Word    PDF


 Research Involving Prisoners

Word    PDF

Application for Research Involving Children

Word    PDF


Application for Research with Cognitively Impaired Persons

Word    PDF


Application for Research Involving Pregnant Women, Human Fetuses, and/or Neonates

Word    PDF


Application for Research Involving Prisoners

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF

IRB Application Guide

Word    PDF


Protection of Human Subjects in HIV/AIDS Related Research

Word    PDF


Investigators and Legally Authorized Representatives

Word    PDF

Waiver of Consent

Waivers, Alterations, and Exceptions to Informed Consent or its Written Documentation

Word    PDF

Request for Waiver of Written Documentation of Informed Consent

Word    PDF


Request for Wavier/Alteration of Informed Consent

Word    PDF


IRB Checklist for Reviewers and Investigators

Word    PDF

Use of Deception/Concealment in Research

Word    PDF

 

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