№ lp_1_14767
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File size: 76 KB
This document is a consent form providing information about participation in a research study involving animals, outlining the risks, benefits, and procedures associated with participation.
Note:
Year
Document Type:
Research Consent Form
Organ / Institution:
Ross University School of Veterinary Medicine
Target Audience:
Animal owners
Price: 8 / 10 USD
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2026
Region / City:
VUMC
Topic:
Scholarship Fund Allocation
Document Type:
Procedural Guide
Institution:
VUMC Office of Research
Author:
VUMC Research Administration
Target Audience:
Center Administrators, PIs, Lab Managers
Effective Period:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Year:
2001
Region / City:
Oceanic voyage
Theme:
Survival, human-animal interaction
Document type:
Literary summary / analysis
Author:
Yann Martel
Target audience:
Readers of "Life of Pi"
Characters:
Pi, Richard Parker, Orange Juice, hyena, zebra
Narrative focus:
Psychological and moral development, animal behavior, human resilience
Events described:
Shipwreck, survival struggles, predator-prey dynamics, emotional and physical challenges
Year:
2025
Jurisdiction:
Namibia, High Court, Main Division, Windhoek
Case Number:
HC-MD-CIV-MOT-REV-2025/00532
Parties:
PIS Security Services CC (Applicant); Chairperson of the Central Procurement Board of Namibia (First Respondent); Chairperson of the Review Panel (Second Respondent); Namibia University of Science and Technology (Third Respondent); Novo Security Services CC (Fourth Respondent); Six Thousand Security Services CC (Fifth Respondent); Chief Nangolo Security Services CC (Sixth Respondent); Minister of Finance (Seventh Respondent)
Coram:
Honourable Acting Justice Corbett
Hearing Date:
29 October 2025
Delivered:
21 November 2025 (Order), 24 December 2025 (Reasons)
Legal Basis:
Public Procurement Act 15 of 2015, s 59(1)
Decision:
Urgent application refused; matter struck from the roll; applicant ordered to pay costs of first and fourth respondents
Document Type:
Court Judgment
Scope:
Review of procurement award and urgent interdictory relief
Year:
Not applicable
Region / City:
Not applicable
Subject:
Research ethics and manuscript submission
Document Type:
Submission Template
Organization / Institution:
Not applicable
Author:
Not applicable
Target Audience:
Researchers, Authors submitting manuscripts
Period of validity:
Not applicable
Approval Date:
Not applicable
Date of Changes:
Not applicable
Note:
Year
Region / City:
Buffalo, NY
Topic:
Research Study Consent
Document Type:
Informed Consent Form
Institution:
University at Buffalo
Author:
University at Buffalo Research Compliance
Target Audience:
Research Participants
Year:
2016
Region / City:
United States
Topic:
Electronic Informed Consent (eIC)
Document Type:
Guidance
Agency / Institution:
Office for Human Research Protection (OHRP), Food and Drug Administration (FDA)
Author:
Office for Human Research Protection (OHRP), FDA
Target Audience:
Researchers, IRBs, Clinical Investigators, and Study Participants
Period of Validity:
Ongoing
Approval Date:
December 2016
Date of Revisions:
Not specified
Year:
2018
Region / City:
United States
Theme:
Cancer prevention, clinical trials
Document Type:
Template
Organ / Institution:
National Cancer Institute (NCI), National Institutes of Health (NIH)
Author:
NCI
Target Audience:
Researchers, clinical trial participants
Period of Validity:
Ongoing
Approval Date:
January 19, 2018
Date of Changes:
N/A
Note:
Year
Topic:
Human Subject Research
Document Type:
Informed Consent Form
Organization / institution:
Coastal Carolina University
Author:
[PI Name]
Target Audience:
Potential research participants
Year:
Not specified
Region / City:
Not specified
Topic:
Research ethics, informed consent
Document Type:
Addendum
Institution / Organization:
Columbia University
Author:
Not specified
Target Audience:
Research participants
Period of validity:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year
Topic:
Research Ethics
Document Type:
Guidelines
Organization / Institution:
EIU IRB
Target Audience:
Researchers, Institutional Review Board Members
Year:
2025
Topic:
Free, Prior and Informed Consent (FPIC)
Document type:
Protocol
Organization / institution:
Blue Action Fund
Author:
Blue Action Fund
Target audience:
NGOs, project developers, indigenous peoples, local communities
Period of validity:
Not specified
Approval date:
Not specified
Date of modifications:
Not specified
Year:
2023
Region / City:
United States
Topic:
Informed Consent, Research Ethics
Document Type:
Research Guidelines
Organization:
U.S. Department of Health and Human Services, Office for Human Research Protections
Author:
Not specified
Target Audience:
Researchers, Institutional Review Board (IRB) members
Validity Period:
Not specified
Approval Date:
Not specified
Date of Last Update:
Not specified
Year:
2016
Region / City:
Dublin
Topic:
Research Consent Forms
Document Type:
Template
Organization:
Trinity College Dublin
Author:
Trinity College Dublin
Target Audience:
Researchers in historical, social, economic or scientific fields
Period of Validity:
Indefinite
Approval Date:
2016
Modification Date:
N/A
Context:
Template for preparing an informed consent form for use in historical, social, economic, or scientific research, ensuring compliance with EU General Data Protection Regulation.
Document type:
Instructional guidance
Subject:
Informed consent forms in clinical research
Context:
Clinical trials involving human participants
Regulatory and ethical framework:
Research ethics and regulatory compliance
Organizations referenced:
Children’s Oncology Group; National Cancer Institute; National Institutes of Health; OCREB
Funding context:
Public funding by the National Cancer Institute
Intended audience:
Consent form authors; clinical trial investigators; participating centres
Geographic scope:
North America
Population referenced:
Children and adolescents with cancer; parents or legal guardians
Related materials:
Provincial informed consent form templates; lay terminology glossary
Year:
2026
Region / City:
Florida, USA
Subject:
Concussion awareness and head injury prevention
Document Type:
Informed consent form
Organization:
Davie Youth Lacrosse Foundation
Target Audience:
Parents/guardians and youth players
Purpose:
Acknowledgement of receipt of concussion information
Legal Requirement:
State of Florida mandatory concussion awareness
Note:
Year
Subject:
Emergency Use Treatment
Document Type:
Informed Consent Form
Year:
2025
Region / City:
N/A
Topic:
Informed Consent, Research Ethics
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
VU HRPP
Author:
N/A
Target Audience:
Research investigators, Institutional Review Boards (IRBs), researchers involved in obtaining informed consent
Effective Period:
Ongoing
Approval Date:
03/03/2025
Revision Date:
None
Year:
2025
Issuing office:
Office of Research Oversight
Organization:
U.S. Department of Veterans Affairs
Administration:
Veterans Health Administration
Document type:
Compliance checklist
Subject area:
Laboratory animal welfare
Regulatory framework:
Animal Welfare Act Regulations, PHS Policy on Humane Care and Use of Animals, VHA Directives
Oversight bodies referenced:
IACUC, ORO, NIH OLAW, USDA APHIS
Scope:
VA research involving live vertebrate animals
Intended users:
VA research facilities and IACUCs
Date of issue:
July 25, 2025
Contact information:
ORO Research Safety and Animal Welfare ([email protected]
Note:
)