№ lp_1_2_35590
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This document is a template for creating a participant debrief sheet for research projects, providing guidelines on content, layout, and ethical considerations in participant debriefing.
Year:
2024
Note:
Region / City
Topic:
Research Ethics, Participant Debriefing
Document Type:
Template
Organization:
University of Cumbria
Author:
Research Team
Target Audience:
Research Participants
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Note:
Year
Document type:
Procurement notification letter and evaluation debrief report
Subject:
Outcome of further competition for the supply of technology products and associated services
Procurement framework:
Crown Commercial Service Technology Products and Associated Services (TePAS) framework
Issuing authority:
Contracting authority participating in the CCS TePAS framework
Addressee:
Tendering supplier
Tender reference:
Procurement reference (not specified)
Procurement title / description:
Supply of technology products and associated services (specified in tender)
Procurement procedure:
Further competition under framework agreement
Evaluation method:
Scoring of tender responses to multiple questions
Evaluation components:
Question-based scoring and total score comparison
Compared parties:
Bidding supplier and successful supplier
Standstill period:
10 days prior to contract award
Attachments:
Debrief report with scoring breakdown and rationale
Signatory:
Contracting authority representative (name not specified)
Note:
Year
Document Type:
Procurement Checklist
Purpose:
Supplier feedback and evaluation documentation
Audience:
Procurement officers and agency staff
Evaluation Criteria:
Technical and financial scoring, preconditions, and weightings
Result:
Preferred supplier identified or no contract awarded
Negotiation Status:
Contract awarded / Not awarded
Key Discussion Points:
Supplier questions and feedback on process
Note:
Year
Topic:
Incident Debriefing
Document Type:
Facilitator Guide
Target Audience:
Service Providers, Emergency Response Teams
Year:
2023
Region / City:
Vanderbilt University
Subject:
Town Hall Feedback
Document Type:
Meeting Minutes
Organization:
Vanderbilt University Student Government Association
Author:
Various Senators
Target Audience:
Vanderbilt University Students
Effective Period:
Fall Semester 2023
Approval Date:
2023-11-18
Date of Changes:
N/A
Type of document:
Template for organizational review
Purpose:
Structured debrief after an incident
Note:
Date of incident
Key considerations:
Location, timing, participants, communication, sensory, accessibility, readiness, other factors
Example questions:
Personal account, feelings, perspectives of others, opportunities for change, support needs, learning outcomes, additional comments
Next steps:
Agreed actions after debrief
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
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]