№ files_lp_4_process_3_104421
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Checklist form for investigators to certify compliance with federal regulations on research involving prisoners, specifying permissible categories of research, consent procedures, and oversight requirements.
Year:
2026
Region / City:
United States
Subject:
Human subjects research involving prisoners
Document Type:
Certification form
Organization / Institution:
Fred Hutchinson Cancer Center IRB
Author:
Principal Investigator (unspecified)
Target Audience:
Investigators conducting research involving prisoners
Protocol Number:
Not specified
FH IRB Number:
Not specified
RG Number:
Not specified
Date:
2026
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2018
Region / city:
Australia
Subject:
Prisoner health care
Document type:
Commissioner’s Operating Policy and Procedure (COPP)
Authority / organization:
Department of Justice
Author:
N/A
Target audience:
Prison staff, Health Services staff
Period of validity:
Ongoing
Approval date:
N/A
Date of amendments:
N/A
Context:
This document outlines the policies and procedures regarding the provision of health care to prisoners in Australian prisons, ensuring that health care services are provided in a timely and culturally appropriate manner, in accordance with public health standards.
Year:
2018
Region / City:
Australia
Theme:
Prisoner communication and privacy policies
Document Type:
Policy
Agency / Organization:
Department of Justice
Author:
Not specified
Target Audience:
Prison staff, legal professionals, prisoners
Period of Validity:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2017
Region / City:
Ruritania
Theme:
Novel, Literature
Document Type:
Novel
Organization / Institution:
Not Applicable
Author:
Kamran Ali Abbasi
Target Audience:
Students, Readers of Classic Novels
Period of Validity:
Ongoing
Approval Date:
17 October 2017
Date of Changes:
Not Applicable
Year:
1983
Region / City:
Maine
Topic:
Prisoner and resident financial management
Document Type:
Policy
Institution:
Department of Corrections
Author:
Commissioner of Corrections
Target Audience:
Employees of the Maine Department of Corrections
Effective Date:
February 14, 1983
Latest Revision Date:
January 7, 2020
Policy Number:
2.12
Applicable Facilities:
All Maine Department of Corrections Facilities
Approval:
Approved by Commissioner
Professional Standards:
Section VII
Authority:
34-A M.R.S.A. Section 3039
Procedures:
Procedures for managing accounts, transactions, and deposits of prisoners and residents
Year:
2018
Region / City:
Australia
Subject:
Prisoner Financial Management
Document Type:
Policy and Procedure
Institution:
Department of Justice
Author:
Not specified
Target Audience:
Prisoners, Correctional Staff, Department of Justice Personnel
Effective Period:
Ongoing
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2026
Region / City:
Pine Ridge Indian Reservation, South Dakota
Theme:
Indigenous Rights, Colonial History, U.S. Government Treaties
Document Type:
Testimonial, Legal and Historical Analysis
Organization / Institution:
Bureau of Indian Affairs
Author:
Mani 9 (Wowitan Yuha, David Swallow, Jr.)
Target Audience:
Native American Communities, Legal Experts, Activists
Period of Application:
1800s - Present
Date of Approval:
1980s
Date of Changes:
1990s
Context:
A historical and legal analysis of the loss of the Black Hills by the Lakota people, highlighting the violation of treaties and their continued struggle for sovereignty and rights over the sacred land.
Year:
1941–1946
Location:
Hampton Lovett, near Droitwich Spa, Worcestershire, United Kingdom
Document type:
Historical camp record and research report excerpt
Subject:
Prisoner of War camp administration and activities during and after the Second World War
Camp designation:
Camp 54 (Hampton Lovett Camp / Longbridge Camp)
Camp category:
Labour and Working Camp
Managing authority:
War Office, Western Command
Inspecting organizations:
International Committee of the Red Cross; Political Intelligence Department of the Foreign Office
Author of research report:
Roger J. C. Thomas
Publishing body of report:
English Heritage
Report year:
2003
Prisoner nationalities:
Italian, Austrian, German
Camp capacity:
Approximately 800 prisoners in 1943
Commandant:
Lt. Col. A. C. F. Foreman
Other officers mentioned:
Major A. Phillips; Major Letch
Period covered by events:
1941–1946
Key activities recorded:
labour deployment, camp administration, inspections, English education classes, political screening, prisoner welfare observations
Associated hostels:
Charlton (Pershore); Clifton (Rugby); Kidderminster; Moor Lane (Willoughby); Pershore; Stoulton (Worcestershire); Woods Lane (Cradley Heath); Alvechurch; Harrington; Mustow Green; Ribbesford (Bewdley); Sillins Lane (Redditch)
Year:
1945–1947
Location:
Luton, Bedfordshire, United Kingdom
Type:
Prisoner of War Camp / German Working Camp
Camp Number:
270
Commandant:
Lt. Col. M.F.F. Buszard, later Lt. Col J.M. Ditmas
Camp Leader:
Uffz Alfred Jahn, later Sold Rudolf Mundt
Deputy Camp Leader:
Uffz Josef Spies
Interpreters:
S/Sgt B Strik
Medical Officers:
St/Arzt Dr H Ludwig, U/Arzt Dr Wilhelm Plump
Capacity:
~500–1250 POWs
Political Screening:
A, B+, C grades assigned to prisoners
Activities:
Library, films, lectures, camp newspaper, religious services, education, entertainment
Oversight:
Political Intelligence Department (PID) / Control Office for Germany and Austria (COGA)
Historical Notes:
Established late 1945, formerly Chrishall Camp, integrated POWs from US camps in 1946, repatriation ongoing until at least mid-1947
Document Type:
Project report / historical record
Source:
English Heritage, Roger J.C. Thomas, 2003
Year:
2013
Country:
United States
Agency:
United States Marshals Service
Department:
U.S. Department of Justice
Document type:
Federal budget justification
Budget category:
Federal Prisoner Detention Appropriation
Publication date:
February 2012
Program activities:
Detention Services; JPATS Transportation
Strategic framework:
DOJ Strategic Goal 3 – Administration of Justice
Estimated average daily detention population:
64,917
Total budget request:
$1,668,235,000
Detention services request:
$1,623,085,000
Transportation request:
$45,150,000
Related organizational change:
Merger of the Office of the Federal Detention Trustee with the U.S. Marshals Service
Scope:
Federal detention operations, prisoner housing, medical care, transportation, and infrastructure
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.
Issuing organization:
National Institutes of Health
Program:
Maximizing Investigators’ Research Award for Early Stage Investigators
Funding mechanism:
R35
Clinical trial policy:
Clinical Trial Optional
Document type:
Application guidance and checklist
Subject area:
Biomedical and behavioral research funding
Target applicants:
Early Stage Investigators
Related documents:
Funding Opportunity Announcement; SF424 (R&R) Research Instructions
Application components:
Forms, narrative attachments, budgets, human subjects and clinical trials information
Formatting requirements:
Font, margins, layout, and hyperlink rules specified
Jurisdiction:
United States
Year:
2023
Region / City:
USA
Subject:
Clinical Research, Financial Disclosure
Document Type:
Form
Organization / Institution:
FDA
Author:
FDA
Target Audience:
Clinical investigators
Effective Period:
Ongoing
Approval Date:
N/A
Date of Changes:
N/A
Year:
2016
Region / city:
Not specified
Subject:
Clinical trial regulations, GCP compliance
Document type:
Checklist
Institution:
Not specified
Author:
Not specified
Target audience:
Investigators, trial staff
Period of validity:
Not specified
Approval date:
Not specified
Date of changes:
Not specified
Year:
2023
Region / city:
N/A
Topic:
Clinical Trial Consent
Document Type:
Research Protocol
Organization / Institution:
DF/HCC
Author:
N/A
Target Audience:
Parents or Guardians of Children Participating in Clinical Trials
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
November 2023
Region / City:
London
Topic:
Research Funding
Document Type:
Policy
Organization:
British Heart Foundation
Author:
British Heart Foundation
Target Audience:
Principal Investigators, Co-applicants, Research Staff
Period of Application:
Until 3 months after the grant end date
Approval Date:
November 2023
Date of Changes:
N/A
Year:
2022
Region / City:
London
Topic:
Clinical Trials, Investigational Medicinal Products, Clinical Development
Document Type:
Template
Organization / Institution:
University College London
Author:
University College London
Target Audience:
Clinical researchers, Investigators, Medical professionals involved in Clinical Trials
Effective Date:
02-Mar-2022
Version:
2.0
Period of Validity:
Reviewed annually
Approval Date:
02-Mar-2022
Date of Last Revision:
Not specified