№ files_lp_4_process_3_104448
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This document provides a template for creating a research study consent form, outlining the information that should be included for participants and the required disclaimers.
Note:
Year
Institution:
Western Washington University
Target Audience:
Researchers, Survey Participants
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Year:
Not specified
Region / City:
Not specified
Theme:
Human Research Protection Program
Document Type:
Table of Contents
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Researchers, Institutional Review Boards (IRBs)
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Context:
A table of contents for a toolkit containing standard operating procedures, forms, templates, and other resources related to human research protection.
Year:
2026
Region / City:
Covenant Medical Center, Texas
Subject:
Research clearance procedures
Document type:
Instructional document
Institution:
TTUHSC, PSJH
Author:
TTUHSC faculty
Target audience:
TTUHSC faculty, researchers
Effective period:
Ongoing
Approval date:
2026
Modification date:
Not specified
Note:
Year
Theme:
Human Research Protection Program (HRPP)
Document type:
Procedure
Target Audience:
HRPP staff, investigators
Year:
2018
Region / City:
N/A
Subject:
Research ethics, human subjects, federal regulations
Document type:
Worksheet
Organization / Institution:
HRPP
Author:
N/A
Target audience:
HRPP staff, Principal Investigators (PIs), IRB members
Period of validity:
Until initial IRB review submission
Approval date:
N/A
Amendment date:
N/A
Year:
Annual (beginning in May)
Subject Area:
Human Research Protection Program (HRPP) oversight and Institutional Review Board (IRB) evaluation
Document Type:
Procedure
Applicable Regulations:
21 CFR §56.106; 21 CFR §56.107; 45 CFR §46.107; 45 CFR §46 Subpart E
Responsible Authority:
Organizational Official
Involved Roles:
IRB Executive Chair; HRPP Administrator; IRB members; IRB Chair; IRB Vice-Chair; HRPP staff
Scope:
Evaluation of HRPP performance, IRB composition, member qualifications, training compliance, and subject outreach program
Key Activities:
Collection of updated résumés or curricula vitae; performance evaluation; review of regulatory compliance and audits; assessment of resources; update of IRB and organizational registrations
External Registry:
Office for Human Research Protections (OHRP) electronic filing system
Review Cycle:
Annual
Outputs:
Written evaluation; corrective and administrative actions; reappointment correspondence
Year:
2025
Region / City:
N/A
Theme:
Human Research Protection Program
Document Type:
Standard Operating Procedure (SOP)
Organization:
West Virginia University (WVU)
Author:
WVU OHRP Director
Target Audience:
Institutional Review Board (IRB) managers and investigators
Effective Period:
Quarterly
Approval Date:
12/15/2025
Revision History:
None
Year:
2026
Institution:
Western Washington University
Document Type:
Administrative Form
Target Audience:
Principal Investigators, Research Staff, Students
Purpose:
Requesting modifications to IRB/HRPP-approved research protocols
Submission Method:
Email attachments only
Compliance:
Federal regulations and university HRPP policy
Required Information:
Protocol number, study title, principal investigator, modification details, supporting materials
Processing Time:
5–7 business days for non-extensive reviews
Instructions:
Complete all applicable sections, attach relevant documents, submit only as Word document
Year:
2025
Region / City:
West Virginia
Topic:
Emergency response, HRPP
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
West Virginia University
Author:
WVU OHRP Director
Target Audience:
Institutional personnel, HRPP staff, researchers
Effective Period:
Ongoing
Approval Date:
12/15/2025
Revision Date:
None
Emergency Response Plans:
Yes
Scope of Document:
Procedures for HRPP emergency response
Related Documents:
HRP-040, HRP-060, HRP-063, HRP-101, HRP-108, HRP-351, HRP-352, HRP-542, HRP-801
Note:
Contextual Description
Year:
2022
Organization:
Human Research Protection Program (HRPP)
Document type:
Guidance / Procedural Notice
Audience:
Human research investigators and research staff
Region:
Not specified
Effective period:
Until further updates or resumption of normal operations
Date issued:
December 9, 2022
Related documents:
HRP-108 - FLOWCHART, HRP-351 - WORKSHEET
Year:
2024
Region / City:
Bellingham, WA
Topic:
Research Study Closure
Document Type:
Form
Organization / Institution:
Western Washington University
Author:
HRPP Office
Target Audience:
Researchers and Investigators
Effective Period:
Ongoing
Approval Date:
Not provided
Date of Last Revision:
Not provided
Year:
2025
Region / City:
USA / WVU
Subject:
Human Research Protection Program Evaluation
Document Type:
Standard Operating Procedure (SOP)
Institution / Organization:
WVU Office of Human Research Protection
Author:
WVU OHRP Director
Target Audience:
IRB members, IRB staff, Institutional Officials, Organizational Officials
Period of Validity:
Annual
Approval Date:
12/15/2025
Revision Date:
None
Year:
2024
Region / City:
Bellingham, Washington
Subject:
Modification Request
Document Type:
Form
Organization / Institution:
Western Washington University
Author:
HRPP
Target Audience:
Principal Investigators, Research Team Members, Students, HRPP Staff
Period of Validity:
Until modifications are approved
Approval Date:
N/A
Modification Date:
N/A
Year:
2026
Region / City:
South Carolina
Topic:
Procurement
Document Type:
Amendment
Organization / Institution:
State of South Carolina
Author:
Ollie Marie Jackson
Target Audience:
Prospective Offerors
Period of Validity:
01/26/2026 - 02/11/2026
Approval Date:
01/26/2026
Amendment Date:
01/26/2026
Year:
1991-2014
Region / City:
UK
Topic:
Labour Market Transitions, Demographic Analysis
Document Type:
Research Supplement
Author:
Not specified
Target Audience:
Researchers, Policy Analysts, Demographers
Period of Validity:
1991-2014
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
2025
Region / City:
United States
Topic:
Maternity care, Infant nutrition
Document Type:
Survey form
Organization:
Centers for Disease Control and Prevention (CDC)
Author:
Centers for Disease Control and Prevention (CDC)
Target Audience:
Hospital staff, specifically those responsible for infant feeding practices
Period of Action:
January 1, 2025 - December 31, 2025
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2024
Region / City:
Alaska
Theme:
Environmental Compliance, Air Quality
Document Type:
Instructional Manual
Organization / Institution:
Alaska Department of Environmental Conservation
Author:
Division of Air Quality
Target Audience:
Permit Holders, Environmental Compliance Officers
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
April 2024
Year:
2026
Region / City:
Online
Topic:
5G, 6G, telecommunications
Document Type:
Meeting agenda and reports
Organization / Institution:
3GPP SA1
Author:
SA1 Chair, 6G Study Rapporteurs, various contributors
Target Audience:
3GPP participants
Period of Activity:
January 2026
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Region / City:
Nairobi, Kenya
Theme:
Gender-based violence, Digital security
Document Type:
Official statement
Institution:
Government of Kenya
Author:
Government of Kenya
Target Audience:
International organizations, policymakers, public
Period of Validity:
Ongoing
Approval Date:
October 15, 2025
Date of Amendments:
October 15, 2025
Institution:
University of Nevada, Las Vegas
College:
Graduate College
Academic year:
2023–2024
Degree program:
Dual Degree Master of Public Health and Doctor of Medicine
Track:
Generalist Track
Delivery format:
Online
Type of document:
Plan of study form
Catalog reference:
2023–24 Graduate Catalog
Total credits required:
47
Required GPA for graduation:
3.00
Course level requirement:
Minimum 50 percent at the 700 level
Internship requirement:
School of Medicine internship
Culminating experience:
EOH 794
Source type:
University academic catalog and degree requirements form