№ lp_1_2_49876
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This form outlines the requirements for submitting an IRB review request for research involving human participants, providing details on the necessary documents, procedures, and permissions required for the approval process.
Note:
Year
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The product description is provided for reference. Actual content and formatting may differ slightly.
Note:
Year
Document type:
Worksheet
Year:
2022
Region:
Massachusetts
Jurisdiction:
United States
Topic:
Chlamydia infection; expedited partner therapy; sexually transmitted infections
Document type:
Clinical advisory
Issuing body:
Massachusetts Department of Public Health
Legal basis:
M.G.L. c. 111 § 121B; 105 CMR 700.003(J); 105 CMR 721.000
Target audience:
Healthcare providers and pharmacists
Standard treatment referenced:
Doxycycline; azithromycin
Population referenced:
Adolescents, young adults, men who have sex with men
Date of update:
January 28, 2022
Affidavit in Reply to Application for Protection Order / Expedited Order / Mandatory Treatment Order
Year:
2024
Region / City:
Singapore
Subject:
Protection Order, Mandatory Treatment Order, Legal Proceedings
Document Type:
Affidavit
Authority / Institution:
Family Justice Courts of the Republic of Singapore
Author:
(name of respondent or third party)
Target Audience:
Legal professionals, individuals involved in legal proceedings related to harassment
Period of validity:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Note:
Year
Subject:
Research Ethics, Human Subjects, IRB Review
Document Type:
Application Form
Organization / Institution:
University of Mary Washington
Target Audience:
Researchers, Faculty, Students
Year:
2023
Region / City:
Murrieta, CA
Subject:
Electrical Vehicle Charging Station Permit
Document Type:
Checklist
Organization / Institution:
City of Murrieta - Development Services Department
Author:
City of Murrieta - Development Services Department
Target Audience:
Contractors, Engineers, Building Authorities
Period of Validity:
N/A
Approval Date:
N/A
Modification Date:
N/A
Year:
Not specified
Region / City:
Not specified
Theme:
Research involving federal funding or support
Document type:
Research protocol submission
Organization / Institution:
KUMC Institutional Review Board
Author:
Not specified
Target audience:
Researchers applying for expedited review under federal funding or support
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Institution:
University of Oregon
Office:
Research Compliance Services
Document type:
Checklist
Subject area:
Human subjects research
Review types:
Expedited review; Full board review
Submission system:
Research Administration Portal (RAP)
Intended audience:
Investigators submitting human subjects research protocols
Associated forms and appendices:
COI forms; Funding and Sponsorship Form; Research Plan; Appendices A–E; supplemental and collaboration materials
Contact information:
[email protected]
Note:
; 541-346-2510
Year:
2024-2025
Region / City:
United States
Topic:
Special Education Data Collection
Document Type:
Technical Guide
Organization / Institution:
U.S. Department of Education
Author:
Brandon Scott (Contracting Officer’s Representative)
Target Audience:
State Educational Agencies (SEAs), Local Educational Agencies (LEAs)
Effective Period:
SY 2024-25
Approval Date:
Not specified
Modification Date:
May 2025 (Version 21.0)
Year:
2024-25
Region / City:
United States
Subject:
Education
Document Type:
Technical Guide
Organization / Institution:
U.S. Department of Education
Author:
U.S. Department of Education
Target Audience:
State Educational Agencies, Educational Data Stewards
Effective Period:
2024-25
Approval Date:
Not provided
Amendment Date:
Not provided
Year:
2025
Region / City:
San Francisco, CA
Topic:
Immigration Law
Document Type:
Legal Template
Agency / Institution:
United States Department of Justice, Executive Office for Immigration Review
Author:
National Immigration Project
Target Audience:
Immigration Attorneys and Legal Practitioners
Effective Period:
February 28, 2025
Approval Date:
February 28, 2025
Year:
2017
Location:
Grady Health System
Topic:
Chlamydia Treatment, Expedited Partner Therapy (EPT)
Document Type:
Interview Guide
Author:
N/A
Target Audience:
Healthcare providers (MDs, RNs, APNs, residents, etc.)
Period of Application:
N/A
Date of Approval:
N/A
Date of Changes:
N/A
Year:
MM/DD/YYYY
Region / City:
N/A
Theme:
Communications Management
Document Type:
Plan
Institution:
Centers for Medicare & Medicaid Services
Author:
N/A
Target Audience:
Project managers, project team, project sponsor, senior leaders, stakeholders
Period of validity:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
MM/DD/YYYY
Region / City:
N/A
Topic:
Subcontractor Management
Document Type:
Template
Organization:
Centers for Medicare & Medicaid Services (CMS)
Author:
N/A
Target Audience:
Project teams and stakeholders involved in subcontractor management
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2026
Institution:
University of Kansas Medical Center (KUMC)
Document Type:
IRB Request Form / Research Protocol Submission
Target Audience:
Principal Investigators and Research Staff
Applicable Regulations:
45 CFR 46, 34 CFR 97, HHS Common Rule
Research Type:
Minimal Risk Behavioral and Biomedical Studies, Secondary Data Analysis
Submission Method:
myIRB Electronic Application
Required Materials:
Completed Form, Data Collection Sheets, Consent Forms, Recruitment Materials
Notes:
Includes guidance for flexible IRB review eligibility and types of research activities
Note:
Year
Subject:
IRB Member Performance Evaluation
Document Type:
Worksheet
Organization / Institution:
University of Miami
Target Audience:
IRB Chairs, IRB Managers
Period of Effectiveness:
Annual
Document type:
Institutional review form
Organization:
University of New England Institutional Review Board
Jurisdiction:
United States
Scope:
International human subjects research
Applicable research formats:
In-person research; Online-only research
Intended submitter:
Principal Investigator
Regulatory framework:
U.S. federal human subjects research regulations
Review body:
Institutional Review Board
Contact information:
[email protected]
Version date field:
Yes
IRB number field:
Yes
Target audience:
Faculty, staff, and student researchers
Geographic focus:
Research conducted outside the United States
Compliance topics:
Ethics approval, informed consent, data protection, export control regulations
Note:
Year
Document type:
Checklist
Target audience:
Investigators, IRB staff
Context description:
A checklist for investigators and IRB staff to assess and ensure regulatory compliance in clinical and non-clinical research studies.
Year:
2025
Region / City:
Louisiana
Topic:
Alcohol and Drug Survey
Document Type:
Guidelines
Organization / Institution:
Louisiana Board of Regents
Author:
Dr. Allison Smith
Target Audience:
IRB administrators, researchers, university staff
Period of Validity:
2025
Approval Date:
October 4, 2024
Amendment Date:
November 15, 2024