№ files_lp_3_process_7_091834
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The document is a Change Request detailing updates to the OpenAPI definitions for the PM control NRM fragment in 3GPP Rel-16.
Year:
2020
Region / City:
Global
Topic:
Technical specification
Document type:
Change Request
Organization / Institution:
3GPP
Author:
Nokia, Nokia Shanghai Bell
Target audience:
Technical stakeholders in 3GPP
Effective period:
2020-05-15 onwards
Approval date:
2020-05-15
Amendment date:
None
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Year:
2026
Region / City:
India
Topic:
Change Request
Document Type:
CR Form
Organization / Institution:
3GPP
Author:
Huawei
Target Audience:
Working Group
Period of Validity:
N/A
Approval Date:
2026-01-25
Modification Date:
N/A
Change Category:
F (correction)
Release Version:
Rel-20
Work Item Code:
AdNRM_Ph4-OAM
Clauses Affected:
TS28541_GenericRanNrm.yaml
Other Specifications Affected:
Core Network, Radio Access Network
Other Comments:
Forge MR link available
Note:
Context Description
Year:
2025
Region / City:
Sophia Antipolis, France
Theme:
Telecommunications, Network Resource Management
Document Type:
Technical Specification
Organization / Institution:
3rd Generation Partnership Project (3GPP)
Author:
3GPP
Target Audience:
Telecommunication professionals, network engineers
Effective Period:
From March 6, 2025
Approval Date:
March 6, 2025
Change Date:
Not applicable
Specification number:
3GPP TS 28.623
Version:
16.19.0
Release:
16
Publication date:
2025-03-06
Standardization body:
3rd Generation Partnership Project (3GPP)
Technical Specification Group:
Services and System Aspects
Series:
28.62x Generic Network Resources IRP
Subject:
Telecommunication management
Scope:
Solution Set definitions for Generic NRM IRP
Related specification:
3GPP TS 28.622
Annexes:
CORBA, XML, OpenAPI, YANG definitions
Intellectual property notice:
© 2025 3GPP Organizational Partners
Status:
Technical Specification under change control
Year:
2026
Region / City:
India
Topic:
Change Request, Technical Specifications
Document Type:
Change Request
Organization / Institution:
3GPP
Author:
Huawei
Target Audience:
Technical Working Group, Industry Professionals
Period of Validity:
2026-01-24 to ongoing
Approval Date:
2026-01-24
Change History Date:
2026-01-24
Category:
F (correction)
Release:
Rel-20
Work Item Code:
TEI20
Source to WG:
Huawei
Source to TSG:
S5
Affected Clauses:
YAML file updates in TS28623_MnSRegistryNrm.yaml
Other Specifications Affected:
None
Year:
2026
Region / City:
India
Document Type:
Change Request
Organization / Committee:
3GPP TSG-SA5
Author:
Huawei
Work Item Code:
TEI19
Release:
Rel-19
Category:
C
Date Submitted:
2026-01-10
Meeting Number:
165
Clauses Affected:
TraceControlNrm.yaml
Related Specifications:
Other core specifications, Test specifications, O&M Specifications
Revision History:
1st Change at commit 09d56814c19dc9ad803b1dd962315a850f929df4
URL:
https://www.3gpp.org/Change-Requests
Meeting:
3GPP TSG-SA5 #165
Location:
India
Date:
9th Feb 2026 - 13th Feb 2026
CR Form Version:
v12.5
Work Item Code:
TEI20
Source to WG:
Huawei
Source to TSG:
S5
Category:
F (correction)
Release:
Rel-20
Affected Systems:
UICC apps, ME, Radio Access Network, Core Network
Clauses Affected:
TS28623_ExternalDataMgmtNrm.yaml, TS28623_ManagementDataCollectionNrm.yaml, TS28623_MnSRegistryNrm.yaml
Change Date:
2026-01-23
Revision:
1
Summary:
Updates YAML definitions to align ExternalDataType, mgtDataCategory, and SubNetwork-ncO-MnSRegistryNrm with stage2 specifications
Consequences if Not Approved:
Misalignment of YAML definitions with stage2 specification
Forge MR Links:
https://forge.3gpp.org/rep/sa5/MnS/-/merge_requests/2024
Year:
2023
Region / city:
Singapore
Topic:
Protein structure, drug discovery
Document type:
Research article
Organization / institution:
Experimental Therapeutics Centre, Agency for Science, Technology and Research, Singapore
Author:
Yan Li, Ying Lei Wong, Michelle Yueqi Lee, Hui Qi Ng, CongBao Kang
Target audience:
Researchers, scientists in biochemistry and pharmacology
Period of validity:
N/A
Date of approval:
N/A
Date of changes:
N/A
Year:
2012
Region / city:
CDC
Topic:
Molecular Epidemiology, Genotyping
Document type:
Protocol
Organization:
CDC
Author:
CDC
Target audience:
Laboratories, Research Institutions
Period of validity:
N/A
Approval date:
03/06/2012
Date of amendments:
N/A
Purpose:
Amplification of 2 fragments from the rubella virus (RuV) envelope protein 1 (E1) coding region
PCR product sizes:
Fragment 1 (480 nts), Fragment 2 (633 nts)
Required equipment:
Thermocycler, Micropipettors, Class II biological safety cabinet
RNA preparation:
Extraction from clinical samples or cell cultures
Primers:
RV8633, RV8945, RV9112, RV9577
Control RNA:
Dried rubella RNA control
Handling instructions:
Store primers and control RNA at specified temperatures, prepare working solutions before use
Safety recommendations:
Use dedicated equipment and workspaces for RNA procedures
Contextual description:
Protocol for Rubella virus genotyping using RT-PCR to amplify specific RNA fragments, primarily for molecular epidemiological research.
Year:
2020
Meeting:
3GPP TSG-SA5 #131-e
Date:
25 May 2020 – 3 June 2020
Work item code:
SON_5G, EE_5G
Source organizations:
Huawei, Orange, Intel
Target group:
S5
Category:
B (addition of feature)
Release:
Rel-16
Clauses affected:
C.4.3, D.4.3, E.5.16, E.5.19, E.5.20, E.5.x1–E.5.x7
Proposed change affects:
UICC apps, ME, Radio Access Network, Core Network
Reason for change:
Addition of new IOCs and attribute definitions to manage distributed and centralized SON functions
Summary of change:
Add stage 3 solution sets for the SON NRM
Consequences if not approved:
Management of SON functions would not be possible
Related CRs:
S5-203316 (stage2), S5-203371 (stage3)
Revision history:
First change C.4.3 XML schema "nRNrm.xsd"
Year:
2023
Region / city:
Rockville, MD, United States; Ottawa, ON, Canada
Topic:
NMR assignments, antibody research, protein expression
Document type:
Research article
Institution:
Institute for Bioscience and Biotechnology Research, National Institute of Standards and Technology, University of Maryland; Centre for Oncology, Radiopharmaceuticals and Research, Biologics and Radiotherapeutic Drugs Directorate, Health Canada
Author:
Tsega L. Solomon, Kinlin Chao, Genevieve Gingras, Yves Aubin, William B. O’Dell, John P. Marino, Robert G. Brinson
Target audience:
Researchers in biochemistry, protein chemistry, pharmaceutical sciences
Effective period:
2023 and onwards
Approval date:
N/A
Date of changes:
N/A
Keywords:
backbone assignments, Fab domain, NISTmAb, biologics, monoclonal antibodies
Context description:
This document presents the results of a study on the backbone NMR assignments of the yeast-expressed Fab fragment of the NISTmAb antibody, aimed at advancing structural characterization techniques for monoclonal antibodies.
Note:
Year
Subject:
DNA analysis, Electrophoresis
Document Type:
Scientific Procedure, Experimental Data
Author:
Daniel Hering
Target Audience:
Scientists, Forensic Analysts, Students