№ lp_2_2_02539
File format: docx
Character count: 19392
File size: 61 KB
This guidance document provides practical instructions for obtaining informed consent from child participants in paediatric clinical trials, in accordance with Australian research ethics and governance standards.
Year:
2016
Region / city:
Australia
Theme:
Paediatric research ethics and governance
Document type:
Guidance document
Organization / institution:
Australian Paediatric Research Ethics & Governance Network
Author:
Australian Paediatric Research Ethics & Governance Network
Target audience:
Researchers, clinical trial investigators, sponsors
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2025
Region / City:
Irvine, California
Topic:
Human Research Protection, IRB, FDA Compliance, HIPAA
Document Type:
Letter
Institution:
University of California, Irvine
Author:
UC Irvine Investigators
Target Audience:
Study sponsors, UC Irvine researchers
Effective Period:
Ongoing
Approval Date:
January 31, 2003
Amendment Date:
September 15, 2025
Special Thanks to 2021 Sponsors, Advertisers, Contributors, and Ticket Buyers as of January 22, 2022
Year:
2021
Region:
United States
Type of Document:
Acknowledgment / Donor List
Organizations:
Multiple local businesses and institutions
Contributors:
Individuals and companies listed with contributions
Amounts:
Detailed in USD for sponsorships, donations, advertising, endowments, and trade
Date Compiled:
January 22, 2022
Endowment Contributions Period:
2016–2021
Categories:
Sponsorship, donation, advertising, trade, endowment
Note:
Year
Subject:
Child and Adult Care Food Program (CACFP)
Document Type:
Checklist
Organization / Institution:
Tennessee Department of Human Services
Target Audience:
Sponsoring organizations and individuals renewing or applying for the CACFP
Context:
A checklist to assess the viability, capability, and accountability of organizations applying or renewing for the Child and Adult Care Food Program (CACFP).
Applies to:
Center-Based Sponsors
Sponsor Name:
[Not specified]
Date Created/ Revised:
[Not specified]
Type of Document:
Procedure / Policy
Program:
CACFP, Summer Food Service Program, National School Lunch Program
Responsible Position:
Position Title in CNPweb
Documentation:
Invoices, receipts, time and attendance reports, payroll records
Software:
[Software Name]
Expense Tracking:
ODE CNP Expense Report
Scope:
Food service operations for enrolled participants
Verification Method:
Double check and allocation per approved budget
Frequency:
Weekly / Monthly / Bi-monthly (as applicable)
Year:
2020
Region / City:
Not specified
Topic:
Sponsorship and donations
Document type:
Financial report
Organization / Institution:
National Football Foundation (NFF)
Author:
Not specified
Target audience:
Sponsors, donors, and event participants
Period of validity:
2020
Approval date:
Not specified
Date of changes:
Not specified
Year:
2023
Region / city:
England and Wales
Topic:
NHS Research, Sponsorship, Study Setup
Document Type:
Template email
Organisation:
NHS, Sponsor organisation
Author:
Not specified
Target audience:
Sponsors, NHS organisations, Research teams
Effective period:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Date:
March 20, 2023
Location:
Washington, DC
Event Name:
Covid Litigation Conference (CLC 2023)
Event Dates:
March 25–26, 2023
Event Location:
Atlanta, Georgia
Organizers:
The Vaccine Safety Research Foundation (VSRF); Mendenhall Law Group
Sponsors and Partners:
Children’s Health Defense; The Front Line COVID-19 Critical Care Alliance (FLCCC); No College Mandates; The Unity Project
Type of Document:
Press release
Subject:
Announcement of sponsors, partners, speakers, and program details for a legal conference focused on Covid-related litigation
Primary Audience:
Attorneys
Additional Audience:
General public; Journalists
Continuing Legal Education:
Eleven hours of CLE credit applied for in 20 states
Media Contact:
Trevor FitzGibbon
Contact Information:
704-775-0487; [email protected]
Distribution:
For immediate release
Year:
2024
Region / City:
Ontario
Subject:
Clinical Trials, Pharmaceutical Agreements
Document Type:
Amending Agreement
Organization / Institution:
CTO
Author:
CTO
Target Audience:
Pharmaceutical Sponsors, Clinical Trial Institutions
Effective Date:
[Insert Date]
Amendment Date:
[Insert Date]
Modification Date:
[Insert Date]
Year:
2024
Region / City:
Washington
Topic:
Food Services, Child Nutrition
Document Type:
Checklist
Organization / Institution:
Office of Superintendent of Public Instruction (OSPI)
Author:
OSPI Child Nutrition Services
Target Audience:
Sponsors of Summer Food Service Program
Period of Validity:
Summer 2024
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2023
Region / City:
Washington State
Subject:
Furlough Sponsorship Responsibilities
Document Type:
Official Form
Organ / Institution:
Department of Corrections
Author:
Department of Corrections
Target Audience:
Furlough Sponsors, Case Managers
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2023
Region / City:
Alberta, Canada
Theme:
Youth programs, Sponsorship
Document Type:
Acknowledgment letter
Organization / Institution:
4-H Alberta
Author:
4-H Alberta
Target Audience:
General Public, Sponsors, Partners
Effective Period:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2026
Region / city:
Northern Ireland
Topic:
Commercial Sponsorship, Local Information Pack, Clinical Research
Document Type:
Template Email
Organization / Institution:
Sponsor organization
Author:
Sponsor organization
Target Audience:
HSC organisations, Principal Investigators, Research & Development offices
Action Period:
Not specified
Approval Date:
Not specified
Modification Date:
Not specified
Organization:
Global Power Networks (GPN)
Program:
Residual Income Success Plan
Industry:
Network Marketing / MLM
Type of Document:
Promotional Email Templates
Purpose:
Recruitment and Re-engagement Communication
Referenced Media:
The Network Marketing Magazine (TNMM) Podcast
Referenced Person:
Denis Vachon
Target Audience:
Upline leaders, past sponsors, former downline members
Format:
Email scripts with follow-up text message templates
Call to Action:
Invitation to connect with Denis Vachon and explore collaboration
Distribution Method:
Email and SMS
Primary Topic:
Business expansion through multi-level marketing platform alignment
Document type:
Application form
Regulatory authority:
South African Health Products Regulatory Authority (SAHPRA)
Country:
South Africa
Subject:
Additions and/or changes in investigators and clinical trial sites
Document number:
GLF-CEM-CT-01D
Related form:
CTF3
Version:
v4
Date of first approval:
October 2019
Date of latest update:
September 2022
Update history:
October 2019 first version approved; March 2020 administrative changes; September 2022 administrative changes, checklist update, appendix removal, document number change
Applicable actions:
Additional investigator(s); Change of investigator(s); Additional site(s); Change in site location
Required attachments:
Cover letter; Investigator documents; Site staff documents; Proof of payment
Approval bodies referenced:
Ethics Committee(s)
Intended applicant:
Sponsor, CRO, or local sponsor company
Regulated area:
Clinical trials
Note:
Year
Topic:
Financial Disclosure
Document Type:
Form
Organization / Institution:
Study Sponsor
Target Audience:
Clinical Investigators, Sub-Investigators
Year:
2024
Region / City:
USA
Topic:
Clinical Research, Regulatory Compliance
Document Type:
Guidance Document
Author:
OVPRI Regulatory Affairs
Target Audience:
Principal Investigators, Research Administrators, Clinical Research Coordinators
Period of Effectiveness:
N/A
Approval Date:
04/25/2024
Amendment Date:
07/09/2024
Description:
Guidance document detailing the steps and regulatory requirements for transferring clinical studies between principal investigators, including documentation updates and approvals required for drug, device, and investigator-initiated studies.