№ lp_1_2_27483
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This document outlines the responsibilities and requirements for individuals wishing to collaborate with University of Virginia researchers in human subjects research.
Year:
2026
Region / City:
Charlottesville, VA
Theme:
Human Subjects Research, Ethical Guidelines, Collaboration
Document Type:
Agreement
Organization / Institution:
University of Virginia
Author:
University of Virginia
Target Audience:
Unaffiliated Collaborating Investigators, Principal Investigators
Effective Period:
Ongoing
Approval Date:
2026-02-08
Date of Last Update:
N/A
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Institution:
Yale University; Yale New Haven Health System
Document type:
Administrative request form
Subject area:
Human subjects research oversight
Regulatory framework:
U.S. federal human research protection regulations
Responsible body:
Institutional Review Board
Related system:
IRES IRB
Intended users:
Principal Investigators; Unaffiliated Investigators
Scope:
Authorization and oversight of unaffiliated investigators
Jurisdiction:
United States
Ethical standards referenced:
Belmont Report; HHS 45 CFR 46; FDA 21 CFR 50; HIPAA
Approval authority:
Yale/YNHHS Institutional Signatory Official
Year:
2026
Location:
Mundole Equestrian, Forres
Topic:
Unaffiliated Dressage Competition
Document Type:
Event Information
Organizing Entity:
Moray Riding Club
Author:
Moray Riding Club
Target Audience:
Riders and participants in dressage events
Date of Event:
22nd February 2026
Deadline for Entries:
17th February 2026
Entry Fees:
£10.00 per class for members, £12.50 per class for non-members
Privacy Notice:
Personal information will be shared for BRC membership benefits and event updates
Event Registration:
Email submission and BACs payment required
Entry Form:
Required
Website:
www.morayridingclub.org
Social Media:
Moray Riding Club Facebook page
Note:
Context Description
Year:
2019
Region / City:
Somerset, Stretcholt
Theme:
Equestrian events, Dressage
Document Type:
Event schedule
Organization:
Stretcholt Equestrian Centre
Author:
Stretcholt Equestrian Centre
Target Audience:
Equestrian competitors and enthusiasts
Period of Validity:
2019 - 2020
Approval Date:
Not specified
Amendment Date:
Not specified
Event Dates:
19th October 2019, 16th November 2019, 22nd December 2019, 26th January 2020, 23rd February 2020, 28th March 2020
Entry Deadline:
Five days prior to each individual event
Entry Fee:
£12 per class
Late Entry Fee:
£14 per class
Eligibility Restrictions:
Specific classes restricted by BD points
Competition Rules:
British Dressage rules
Prizes:
Sponsored by Goodbye Fly
Location:
Stretcholt Equestrian Centre, Somerset
Facilities:
Indoor geltrack surface, outdoor geltrack arena, viewing gallery
Sponsorship:
A&L Hay and Straw Services
Contact Information:
Email – [email protected]
Note:
, Tel – 01278 683312
Website:
www.stretcholt-ec.co.uk
Facebook:
Stretcholt Equestrian Centre Facebook page
Withdrawal Policy:
Full refund before entry deadline, no refund after
Insurance:
No liability accepted for accidents or damage
Age Restriction:
Horses/ponies under four years cannot compete
Dogs:
Must be kept on leads
Lunging:
Not allowed in warm-up area, designated lunging area available
Helmet Requirement:
British Safety Standard must be worn when mounted
Year:
2023
Region / City:
Detroit, MI
Topic:
Convention, Advocacy, Blindness, Empowerment
Document Type:
Event Program
Organization:
National Federation of the Blind of Michigan
Author:
Robert Parsons, Jr.
Target Audience:
Blind individuals, Federation members, Advocates
Period of Activity:
November 10-12, 2023
Approval Date:
November 2023
Date of Changes:
N/A
Note:
Description of Document
Year:
2020
Region / City:
Guelph, Ontario, Canada
Topic:
Material Transfer Agreement, Research Collaboration
Document Type:
Legal Agreement
Organization / Institution:
University of Guelph
Author:
Research Innovation Office, University of Guelph
Target Audience:
University of Guelph faculty, recipient scientists, technology transfer offices
Effective Date:
2020-XX-XX
Expiration Date:
2023-XX-XX
Year:
2023
Region / City:
Europe
Field:
Biomarkers, Clinical Research
Document Type:
Guidelines
Organization:
BioMS-eu
Author:
Michael Khalil
Target Audience:
Researchers, Clinical Laboratories
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Modifications:
Not specified
Context:
This document outlines the procedures and requirements for collaboration in research studies related to biomarkers within the BIOMS-eu network.
Year:
2026
Region / School:
Elmwood Middle School
Topic:
Special Education / Family Engagement
Document Type:
Training Module Outline
Organization:
PACER Center
Author:
Holly Brienza
Target Audience:
Educators and school staff
Estimated Completion Time:
1 hour
Related Legislation:
Every Student Succeeds Act (ESSA), Individuals with Disabilities Education Act (IDEA)
Content Includes:
Emotional responses to disability, roles of families, stressors of daily living, strategies for building relationships and meaningful involvement, references and additional resources
Media:
Video, Audio, PDF, Web links
Year:
2026
Region / City:
United States
Subject:
Technology, Regulatory Enforcement, Policy Development
Document Type:
Guide
Agency / Organization:
[Insert Agency / Organization]
Author:
[Insert Author Name]
Target Audience:
State Regulatory and Enforcement Agencies
Effective Date:
[Insert Date]
Date of Approval:
[Insert Date]
Date of Last Revision:
[Insert Date]
Year:
2026
Institution:
The Chinese University of Hong Kong
Department:
Information Technology Services Centre (ITSC)
Document Type:
Application Form
Intended Users:
CUHK staff (project leaders or LAN administrators)
Purpose:
Request for restricted VPN access for remote support and maintenance
Required Period:
Specified by applicant
Submission Method:
Email with scanned documents
Rules Reference:
Computer Network Policies and Guidelines on Access and Usage
Data Handling:
Personal data collected for identity verification and contact purposes
Processing Time:
Three working days from submission
Endorsing Authority:
Department/Unit Head
Document Type:
Endorsement Certificate
Granting Organization:
Anusandhan National Research Foundation (ANRF), New Delhi
Related Program:
ANRF Interdisciplinary Research Centre
Participating Entities:
Lead Institution and Collaborating Institution
Project Roles:
Principal Investigator (PI) and Co-Principal Investigator(s) (Co-PIs)
Institutional Authority:
University / Institute / Organization / College Administration
Responsible Signatories:
Registrar of University / Head of Institute / Head of Organization / Principal of College
Eligibility Requirement:
Co-Principal Investigators in regular positions with at least six years of service remaining before superannuation
Financial Administration:
Managed by the participating University / Institute / Organization / College
Asset Ownership:
Recorded by the host institution and subject to the discretion of ANRF
Project Funding Source:
Grant-in-aid from Anusandhan National Research Foundation (ANRF)
Project Start Condition:
Begins upon receipt of grant assignment from ANRF
Financial Reporting Requirement:
Settlement of project accounts within three months after project closure
Geographical Reference:
New Delhi, India
Year:
2026
Region / City:
Twin Cities, Minnesota, USA
Theme:
Environmental Conservation, Water Quality, Pollinator Habitat
Document Type:
Project Collaboration Outline
Organization / Institution:
Twin Cities Rotary EcoClub
Author:
Steve Solbrack
Potential Partners:
Mississippi Park Connection, National Park Service, Monarch Joint Venture, Environmental Sustainability Rotary Action Group (ESRAG), Freshwater Society, Rotary Clubs with Environmental Focus, US Fish & Wildlife Service, Friends of the Mississippi River, Mississippi Watershed Management Organization, Minnesota Department of Natural Resources, Three Rivers Park District, The Nature Conservancy
Target Audience:
Environmental organizations, Rotary Club members, community partners
Document Update Date:
September 30, 2025
Related Events:
Earth Day 2026
Scope:
Multi-district collaboration in Minnesota for environmental projects
Year:
20____
Region / City:
Randall County, Texas
Topic:
Legal Procedure
Document Type:
Motion
Organ / Institution:
Randall County District Court
Author:
[Attorney for Defendant]
Target Audience:
Legal Professionals, Court Officials
Period of Effectiveness:
From the date of approval
Date of Approval:
[DATE OF CASE ASSIGNMENT]
Date of Changes:
None indicated
Context:
This is a legal document requesting the appointment of a private investigator to assist a defendant in preparing a defense in a criminal case.
Note:
Year
Subject:
Clinical Trials, Medical Research
Document Type:
Template
Organization / Institution:
EU Clinical Trials Expert Group
Target Audience:
Sponsors of clinical trials
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:
Doha, Qatar
Topic:
Human Research Protection
Document Type:
Manual
Institution:
Virginia Commonwealth University
Author:
Huron Consulting Group
Target Audience:
Researchers, Investigators, Staff
Approval Date:
08/07/2025
Modification Date:
Not specified
Period of validity:
Not specified
Note:
Study Summary 1.1 Please provide a brief summary of the study in the table below. A complete description of the study with detailed information should be provided in the body of the protocol. For sections not applicable to the study, mark them as N/A. Study Title Study Design Primary Objective/Purpose Secondary Objective(s)/Purposes Research Intervention(s) ClinicalTrials.gov NCT # Study Population Sample Size Study Duration for individual subjects Study Specific Abbreviations/ Definitions
Background 3.1 Provide the scientific or scholarly background for, rationale for, and significance of the research based on the existing literature and how will it add to existing knowledge. :
this section should be limited to only information directly related to the research questions and objectives. Do not include your full dissertation proposal. 3.2 Describe any relevant preliminary data (e.g. pilot data).
Procedures Involved 5.1 Describe and explain the study design. 5.2 Please select the methods that will be employed in this study (select all that apply):
☐ Audio/Video Recording ☐ Psychophysiological Recording ☐ Behavioral Interventions ☐ Record Review - Educational ☐ Behavioral Observations and Experimentations ☐ Record Review - Employee ☐ Deception ☐ Record Review- Medical ☐ Focus Groups ☐ Record Review - Other ☐ Interviews ☐ Specimen Collection or Analysis ☐ Investigational Medical Device – (e.g. Medical Mobile Applications) ☐ Surveys and/or Questionnaires ☐Psychometric Testing ☐ Other Social-Behavioral Procedures Provide a description of all research procedures being performed and when they are performed. (Upload any surveys, questionnaires, interview scripts, focus group scripts, debriefing scripts, psychometric tests, stimulus materials, intervention manuals, and data collection forms on the Local Site Documents page in the IRB application.) 5.3 Describe the procedures or interventions that are going to be conducted as part of the research project, but that would have been conducted anyway, even if the research was not occurring (i.e. standard of care procedures, activities that would occur in a classroom). 5.4 Describe the procedures performed to lessen the probability or magnitude of risks of items selected in 5.2.5. 5 If accessing or collecting existing data, describe: The data that will be collected during the study (e.g. demographics, medical history, etc.). Attach the data capture sheet(s) on the Local Site Documents page in the IRB application. How the data will be obtained, including how you have the authority to access the data. The source or location of the data (e.g. USF Epic, TGH Epic, Hillsborough County School records, CANVAS records, publicly available databases, etc.). 5.6 If collecting and/or analyzing biological specimens, describe: How the biological specimens will be or have been collected. How the biological specimens will be stored. How long the biological specimens will be stored. How the biological specimens will be used. The laboratories that will be used. Whether the collected biological specimens will undergo genetic testing. If so, indicate if this study is part of a Genome Wide Association Study (GWAS) and whether the data will be forwarded to the NIH dbGaP. 5.7 If there are plans for long-term follow-up (once all research related procedures are complete), what data will be collected during this period.
Data and Specimen Storage for Future Research 6.1 If data or specimens will be banked for future research studies, describe where the data or specimens will be stored, how long it/they will b:
the process to request a release, approvals required for release, who can obtain data or specimens, and the data to be provided with specimens.
Year:
2025
Institution:
Yale University; Yale New Haven Health System
Document type:
Administrative request form
Subject area:
Human subjects research oversight
Regulatory framework:
U.S. federal human research protection regulations
Responsible body:
Institutional Review Board
Related system:
IRES IRB
Intended users:
Principal Investigators; Unaffiliated Investigators
Scope:
Authorization and oversight of unaffiliated investigators
Jurisdiction:
United States
Ethical standards referenced:
Belmont Report; HHS 45 CFR 46; FDA 21 CFR 50; HIPAA
Approval authority:
Yale/YNHHS Institutional Signatory Official
Note:
Year
Document Type:
Clinical Research Delegation Log
Author:
Principal Investigator / Investigator of Record
Target Audience:
Research Staff
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