№ lp_1_28087
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Character count: 43584
File size: 654 KB
Investigator:
Required: [Enter name, title, and telephone number of the Principal Investigator]
Co-Investigators:
Required: [Enter name(s) with title(s) of Co-Investigators if applicable]
Research Coordinator:
Required: [Enter name(s) with title(s) of Research Coordinator here if applicable]
Sponsor/Funding Agencies:
Optional: [If applicable, enter Sponsor / Funding Agencies.]
Protocol number:
Optional: [If applicable, enter protocol number.]
Emergency Contact Number (24 hours / 7 days a week):
Optional: [Required for studies greater than minimal risk: Enter contact number (24 hours / 7 days a week here)]
Year:
[If applicable]
Region / city:
[If applicable]
Topic:
Research study, informed consent
Document type:
Consent form
Organization / institution:
[If applicable]
Author:
[If applicable]
Target audience:
Participants in clinical trials
Period of validity:
[If applicable]
Approval date:
[If applicable]
Modification date:
[If applicable]
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The product description is provided for reference. Actual content and formatting may differ slightly.
Note:
Year
Organization / Institution:
Wilson Workforce and Rehabilitation Center
Target Audience:
Applicants to the Wilson Workforce and Rehabilitation Center
Note:
Year
Institution:
Auckland University of Technology
Year:
2024
Region / City:
Not specified
Topic:
Non-SIT S&A Qualification Testing
Document Type:
Report
Organization / Institution:
Non-SIT S&A QT Team
Author:
Non-SIT S&A QT Team
Target Audience:
Program participants involved in Non-SIT S&A QT
Effective Period:
Not specified
Approval Date:
02-Sep-2024
Amendment Date:
Not specified
Note:
Year
Subject:
Research
Document Type:
Information Sheet
Organization / Institution:
University of Technology Sydney
Author:
[insert name]
Target Audience:
Potential participants in the research study
Period of Activity:
[insert period if available]
Approval Date:
[insert approval date if available]
Date of Amendments:
[insert amendments date if available]
Note:
Year
Organization / Institution:
UN Environment Programme (UNEP)
Target Audience:
Insurance organizations, stakeholders in climate action
Note:
Year
Year:
2024
Region / city:
Birmingham
Topic:
Clinical Research, Participant Engagement, Informed Consent
Document Type:
Standard Operating Procedure (SOP)
Organization / institution:
University of Birmingham
Author:
Not specified
Target audience:
Clinical researchers, Chief Investigators, Clinical Trials Units
Period of validity:
From 2024
Approval date:
Not specified
Revision date:
Not specified
Next review:
2027, Quarter 3 (Jul-Sep)
Year:
2023
Region / city:
Canberra
Theme:
Climate Change, Education, Research
Document type:
Participant Information Sheet
Institution:
The Australian National University
Author:
Chris Browne
Target audience:
ANU students
Period of action:
2023
Approval date:
Not specified
Date of amendments:
Not specified
Note:
Year
Note:
Year
Year:
2023
Region / City:
Diocese / Cathedral
Topic:
Safeguarding, Leadership, Church Practices
Document Type:
Workbook
Author:
Church of England
Target Audience:
Church leaders, safeguarding officers
Period of Effect:
October 2023 onwards
Date of Approval:
October 2023
Date of Changes:
Not specified
Note:
Year
Topic:
Data protection, research ethics, participant consent
Document Type:
Template
Target audience:
Researchers conducting non-health-related studies involving personal data
Year:
2019
State:
Wisconsin
Program:
IRIS
Subject:
One-time expense requests
Document type:
Participant education and acknowledgement form
Form number:
F-01205C
Issuing authority:
Department of Health Services, Division of Medicaid Services
Eligibility criteria:
IRIS program participation requirements
Reviewing body:
Department of Health Services
Required signatories:
Participant, Guardian (if applicable), IRIS Consultant
Year:
2026
Region / city:
United Kingdom
Subject:
Implementation of online support tools for relatives of people with bipolar disorder and psychosis
Document type:
Participant information sheet
Organization / institution:
Lancaster University, University College London, University of Liverpool, NHS Trusts
Author:
IMPART research team
Target audience:
Relatives of patients receiving NHS mental health support
Funding:
National Institute of Health Research (NIHR)
Ethics approval:
NHS Research Ethics Committee
Duration:
Three-year study
Method:
Interviews, audio-recorded with transcription and anonymization
Purpose:
To understand barriers, facilitators, and success factors in the implementation of the REACT toolkit
Data usage:
Inform national implementation plan, academic publication, conference presentation
Emergency Use Authorization Medical Community Leaders Roundtable Participant Bios, November 12, 2021
Date:
November 12, 2021
Event:
Emergency Use Authorization Medical Community Leaders Roundtable
Document type:
Participant biographies
Topic:
Emergency use authorization, COVID-19, public health, clinical research, health policy
Organizations represented:
Infectious Diseases Society of America; American Academy of Pediatrics; Georgetown University; U.S. Food and Drug Administration; University of Utah; ARUP Laboratories; Duke University; American Hospital Association
Participants:
Adarsh Bhimraj, Anne Edwards, Jesse L. Goodman, Kimberly Hanson, Adrian F. Hernandez, Mark A. Howell
Geographic focus:
United States
Professional fields:
Infectious diseases; pediatrics; regulatory science; clinical research; health policy; hospital administration
Note:
File Number
Region / City:
Delaware, New Castle County, Kent County, Sussex County
Theme:
Guardianship, Consent Affidavit
Document Type:
Legal Affidavit
Authority / Institution:
The Family Court of the State of Delaware
Author:
Affiant
Target Audience:
Parents and guardians involved in custody and guardianship matters
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
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
Year:
2020
Region / City:
United Kingdom
Topic:
Patient consent, publication, medical materials
Document Type:
Consent Form
Organization:
British Association of Dermatologists
Author:
Not specified
Target Audience:
Health professionals, researchers, clinicians
Period of validity:
N/A
Approval Date:
April 2020
Modification Date:
N/A
Context:
Consent form for patients or their representatives to allow the British Association of Dermatologists to use medical materials in publications, ensuring anonymity and outlining the terms of usage.
Year:
2016
Region / City:
Wisconsin
Topic:
Background Check Consent
Document Type:
Form
Organization / Institution:
Wisconsin Department of Administration
Author:
Wisconsin Department of Administration
Target Audience:
Job applicants in Wisconsin
Effective Period:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified