№ lp_1_2_16964
File format: docx
Character count: 4273
File size: 97 KB
Checklist detailing required materials and documentation for submitting human subjects research protocols for expedited or full board review within an institutional research compliance framework.
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
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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
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
Institution:
Fred Hutchinson Cancer Center
Affiliated institutions:
University of Washington
Document type:
Model informed consent form
Research domain:
Clinical research
Regulatory framework:
45 CFR 46.116; 21 CFR 50.25
Oversight body:
Fred Hutch IRB; OHRP; FDA
Principal Investigator:
Chris Doe MD PhD
Intended use:
Consent for participation in clinical research studies
Population:
Prospective research participants, parents or guardians, legally authorized representatives
Study phases referenced:
Phase 1; Phase 2; Phase 3
Risk level:
More than minimal risk (when applicable)
Geographic scope:
United States
Language of document:
English
Year:
2024
Region / city:
China, New Zealand, Egypt, Philippines, Arab countries
Theme:
Scientific and technological cooperation, international research projects
Document type:
Agreement, Cooperation guidelines
Organization / institution:
Ministry of Science and Technology of China, New Zealand Ministry of Business, Innovation and Employment, Egyptian Ministry of Higher Education and Scientific Research, Department of Science and Technology of the Philippines
Author:
N/A
Target audience:
Government bodies, research institutions, international cooperation teams
Duration:
2-3 years
Approval date:
2024
Amendment date:
N/A
Document type:
Agreement
Institution:
Oregon State University
Program:
Human Research Protection Program
Oversight body:
Institutional Review Board
Research area:
Human subjects research
Parties:
Individual Investigator; Oregon State University
Compliance framework:
International, federal, state, and local laws and regulations
Training requirements:
Research ethics training; CITI or equivalent
Approval requirement:
Institutional Review Board review and approval
Signature fields:
Investigator; HRPP Administrator