№ lp_1_2_12753
File format: docx
Character count: 48272
File size: 184 KB
Year:
2023
Region / City:
Geneva
Topic:
Internal Oversight, Audit, Risk Management
Document Type:
Annual Report
Organization / Institution:
World Meteorological Organization
Author:
Secretary-General
Target Audience:
WMO Management, External Oversight Bodies
Period of Validity:
2023
Approval Date:
30 May 2024
Date of Amendments:
N/A
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Year:
2025
Region / City:
United States
Topic:
Cloud Services, Market Research
Document Type:
Request for Information (RFI)
Organization:
Department of the Interior (DOI), Interior Business Center (IBC), Acquisition Services Directorate (AQD)
Author:
U.S. Government
Target Audience:
Industry Vendors, Cloud Service Providers
Period of Action:
4th quarter FY2025
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Issuing office:
Office of Research Oversight
Organization:
U.S. Department of Veterans Affairs
Administration:
Veterans Health Administration
Document type:
Compliance checklist
Subject area:
Laboratory animal welfare
Regulatory framework:
Animal Welfare Act Regulations, PHS Policy on Humane Care and Use of Animals, VHA Directives
Oversight bodies referenced:
IACUC, ORO, NIH OLAW, USDA APHIS
Scope:
VA research involving live vertebrate animals
Intended users:
VA research facilities and IACUCs
Date of issue:
July 25, 2025
Contact information:
ORO Research Safety and Animal Welfare ([email protected]
Note:
)
Year:
2021
Region / City:
International
Topic:
Oversight activities in aerospace quality management
Document Type:
Guidelines
Organization:
International Aerospace Quality Group (IAQG)
Author:
IAQG Oversight Committee
Target Audience:
Aerospace certification bodies, auditors, and quality management professionals
Effective Period:
Ongoing
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2025
Region / City:
Washington State
Theme:
Legislative Task Force Meeting
Document Type:
Meeting Agenda
Organization / Institution:
Department of Social and Health Services (DSHS)
Author:
Babs Roberts, Senior Advisor, Programs & Policy, Economic Justice Team
Target Audience:
Task Force Members, Public
Period of Effect:
August 21, 2025
Approval Date:
August 21, 2025
Date of Amendments:
None
Note:
Year
Year:
2026
Region/City:
United States
Topic:
Multifamily Housing Management
Document Type:
Form
Organization/Institution:
HUD
Author:
HUD
Target Audience:
HUD staff, Performance Based Contract Administrators, Traditional Contract Administrators, Mortgagees
Effective Period:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Organization:
Office for Nuclear Regulation
Document type:
Technical Assessment Guide
Issue number:
2
Publication date:
May 2024
Next major review date:
May 2027
Document reference:
CNS-TAST-GD-4.3
Record reference number:
2017/106068
Professional lead:
Protective Security
Author:
Deputy Professional Lead
Approved by:
Professional Lead – Protective Security
Regulatory framework:
Nuclear Industries Security Regulations 2003
Related principles:
Security Assessment Principles; Fundamental Security Principles; SyDP 4.3; FSyP 4
Scope:
Oversight of suppliers of items or services of nuclear security significance
Target audience:
ONR inspectors
Revision history:
Periodic fit for purpose review
Note:
Year
Document Type:
Clinical Research Delegation Log
Author:
Principal Investigator / Investigator of Record
Target Audience:
Research Staff
Year:
2023
Region / City:
Birmingham
Theme:
Clinical Research, Medical Oversight
Document Type:
Standard Operating Procedure (SOP)
Organization / Institution:
University of Birmingham
Author:
Not specified
Target Audience:
Clinical researchers, healthcare professionals
Period of validity:
From the effective date
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2019
Region / city:
United States
Topic:
Cybersecurity, Military Health System
Document type:
Memorandum
Agency / institution:
Defense Health Agency
Author:
Ronald J. Place
Target audience:
Department of Defense officials, military healthcare personnel
Effective period:
2019–2029
Approval date:
2019
Date of amendments:
None
Note:
Year
Topic:
Conflict of Interest, Commitment Management
Document Type:
Management Plan
Organization:
University of Illinois
Author:
Professor XYZ
Target Audience:
University Faculty and Administration
Period of Validity:
Annual
Year:
2022
Region / City:
N/A
Topic:
VA Informed Consent Addendum, NCI CIRB, Boilerplate Language Revision
Document Type:
Guidance
Organization / Institution:
Department of Veterans Affairs (VA)
Author:
ORD, Office of Research Oversight (ORO), NCI CIRB
Target Audience:
VA Facilities, Research Community
Effective Period:
N/A
Approval Date:
April 6, 2022
Date of Updates:
May 12, 2022
Contextual description:
Guidance document on revisions to VA boilerplate language for NCI studies overseen by the NCI CIRB, detailing required actions for VA Facilities.
Note:
Year
Topic:
Human Research, IRB Oversight
Document Type:
Guidance
Target Audience:
Investigators conducting Human Research
Contextual description:
A guidance document for investigators conducting human research, outlining obligations and procedures for IRB oversight and approval.
Year:
2025
Region / City:
Fort Eustis, Virginia
Topic:
Acquisition Management
Document Type:
Pamphlet
Organization / Institution:
U.S. Army Training and Doctrine Command
Author:
David J. Francis
Target Audience:
U.S. Army personnel involved in acquisition management
Period of Validity:
2025 and onward
Approval Date:
16 May 2025
Amendment Date:
N/A
Effective Date:
January 1, 2026
Chapter:
0308
Document Type:
Manual
Region / City:
United States
Thematic Focus:
Nuclear Reactor Security
Institution:
U.S. Nuclear Regulatory Commission (NRC)
Target Audience:
NRC licensees, nuclear reactor operators, security personnel
Date Approved:
January 1, 2026
Effective Date:
10/16/2023
Note:
Region / city
Note:
Year
Note:
Year
Theme:
Biosecurity, Biorisk Management
Document Type:
SOP Template
Organization / Institution:
[Insert Institution/Facility Name]
Target Audience:
Facility personnel, biorisk management teams
Document type:
Accountability log
Scope:
Clinical investigation site
Subject matter:
Investigational medical devices
Regulatory framework:
EU Regulation 2017/745 on Medical Devices (MDR)
Applicable date:
26 May 2021
Version date:
18 August 2021
Responsible organization:
Kliniska Studier Sverige
Responsible network:
National network for clinical investigations with medical devices within Clinical Studies Sweden
Geographical context:
Sweden
Intended setting:
Clinical investigation site(s)
Signatory role:
Principal Investigator
Source category:
Clinical research documentation
Year:
2026
Jurisdiction:
United States
Document Type:
Guidance / Protocol
Agency:
U.S. Department of Education
Applicable Law:
ESEA Title II, Part A
Intended Audience:
State Education Agencies (SEA), Local Education Agencies (LEA), Title II Directors
Topics:
Teacher and school leader preparation, training, recruitment, use of Title II funds, evidence-based activities, continuous improvement, compliance with supplement-not-supplant requirements
Review Type:
Self-assessment and on-site/desk review
Instructions Provided:
Yes
Recommended Participants:
Title II, Part A Director(s)