№ files_lp_4_process_2_81979
File format: docx
Character count: 17010
File size: 61 KB
Year:
2024
Region / City:
Athens, Greece
Topic:
Radio Access Network
Document Type:
Change Request
Organization / Institution:
3GPP
Author:
Apple Inc., Vodafone, AT&T
Target Audience:
Technical Working Group
Effective Period:
February 26th, 2024
Approval Date:
February 26th, 2024
Date of Changes:
February 26th, 2024
Change Request:
A request to modify the operation of 2Rx for XR capable devices in the Radio Access Network, specifically introducing changes in UE behavior after acquiring MIB and SIB1.
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Year:
2026
Location:
Gothenburg, Sweden
Topic:
2Rx XR UE paging capability discussion
Document type:
Meeting contribution / technical report
Organization:
3GPP TSG-RAN WG3
Author:
Moderator (Ericsson)
Audience:
RAN working group members, participating companies
Agenda item:
9.2.1
References:
R3-260441
Companies involved:
Ericsson, Huawei, Samsung, China Telecom, Qualcomm, Nokia, Nokia Shanghai Bell, ZTE
Period of discussion:
9–13 February 2026
Decision status:
For discussion and decision
Technical focus:
UE Paging Capability IE, 2Rx XR UE indication, paging optimization
Standards referenced:
TS 38.331, TS 38.473
Year:
2024
Month:
February
Location of Meeting:
Athens, Greece
Organization:
3GPP
Working Group:
TSG-RAN WG2
Meeting:
TSG-RAN WG2 Meeting #125
Document Type:
Change Request
Specification Affected:
3GPP TS 38.300
Current Specification Version:
18.0.0
Release:
Rel-18
Category:
B (addition of feature)
Work Item Code:
NR_TEI18, NR_XR_enh-Core
Source Organizations:
Apple Inc., Vodafone
Source to TSG:
R2
Affected Clauses:
3.2, 16.x
Related Specifications:
TS/TR 38.306, TS/TR 38.304, TS/TR 38.331
Topic:
2Rx XR User Equipment definition and access behavior in NR networks
Reason for Change:
Introduce 2Rx XR UEs to Rel-18
Summary of Change:
Addition of a definition for 2Rx XR UEs and a new clause describing their access and camping behaviour
Approval Consequence:
Lack of support for 2Rx XR UEs in the specification
Year:
2020
Region / City:
Rochester, MN
Topic:
Cybersecurity of medical and research devices
Document type:
Vendor packet
Organization / Institution:
Mayo Clinic
Author:
Mayo Clinic
Target audience:
Vendors, healthcare technology management teams
Period of validity:
N/A
Approval date:
N/A
Date of amendments:
N/A
Year:
2025
Region / city:
EU
Topic:
Health Technology Assessment
Document Type:
Guidance
Organization / Institution:
HTA CG
Author:
European Commission
Target audience:
Professionals in Health Technology Assessment
Validity period:
From 28 NOVEMBER 2025
Approval date:
28 NOVEMBER 2025
Amendment date:
Not specified
Year:
2023
Region / City:
Global
Topic:
Internet of Things, IoT Device Testing
Document Type:
Industry Specification
Organization / Institution:
GSMA
Author:
GSMA
Target Audience:
Mobile Network Operators, IoT Service Providers, IoT Device Makers, IoT Device Application Developers, Communication Module Vendors, Radio Baseband Chipset Vendors
Validity Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Description:
Industry specification document outlining test cases for IoT device compliance with GSMA IoT Device Connection Efficiency Guidelines, focusing on device behavior and network resource management.
Note:
Year
Document type:
Worksheet
Year:
2025
Region / city:
Global
Topic:
Internet of Things (IoT)
Document Type:
Industry Specification
Organization / Institution:
GSM Association
Author:
GSM Association
Target audience:
Mobile Network Operators, IoT Device Manufacturers, IoT Device Application Developers
Period of validity:
Ongoing
Approval date:
May 2025
Date of changes:
Not specified
Year:
2025
Region / City:
United Kingdom
Topic:
COVID-19 treatment, lateral flow device tests
Document Type:
Service Specification
Organization / Institution:
NHS England
Author:
NHS England
Target Audience:
Pharmacy contractors, healthcare professionals
Period of Validity:
Ongoing, from 6 November 2023
Date of Approval:
May 2025
Date of Changes:
01 May 2025
Note:
Year
Subject:
Emergency Use Treatment
Document Type:
Informed Consent Form
HDA Standard Pharmaceutical (Rx-only) Product and Medical Device Information Short Form Instructions
Note:
Year
Theme:
Pharmaceutical products, Medical devices
Document type:
Instructions, Form
Organization / Institution:
HDA
Target audience:
Distributors, Manufacturers, Supply chain professionals
Year:
XXXX
Region / City:
XXX
Theme:
Post-market Surveillance
Document Type:
Report
Organization:
XXX
Author:
XXX
Target Audience:
Regulatory Authorities, Healthcare Professionals
Period of Validity:
[start date] - [end date]
Approval Date:
YYYY-MM-DD
Revision Date:
YYYY-MM-DD
Year:
YYYY
Region / City:
[City/Region]
Topic:
Medical Device Safety and Performance Monitoring
Document Type:
PMCF Plan
Organization:
[Manufacturer Name]
Author:
[Author Name]
Target Audience:
Regulatory Authorities, Medical Device Manufacturers
Validity Period:
YYYY/MM/DD to YYYY/MM/DD
Approval Date:
DD/MM/YYYY
Revision Date:
XXXX
Date of Changes:
YYYY/MM/DD
Year:
2020
Region / city:
Not specified
Theme:
Defense, Technology Development
Document Type:
Statement of Objectives
Organization / Institution:
Not specified
Author:
Not specified
Target Audience:
Defense contractors, technology developers
Period of validity:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Note:
Year
Subject:
Contraception, Medical Procedure
Document Type:
Patient Information and Consent Form
Target Audience:
Patients, Healthcare Providers
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:
2021
Region / City:
United States
Topic:
Pharmaceutical and Medical Device Product Information
Document Type:
Instructional Form
Organization / Institution:
Health Distribution Alliance (HDA)
Author:
Health Distribution Alliance
Target Audience:
Pharmaceutical distributors, medical device manufacturers, suppliers
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
2021