№ lp_1_31869
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Character count: 8457
File size: 81 KB
eCall is a service aimed at providing emergency response in the European Union, requiring specific numbering resources for its implementation and operation across all new passenger cars, ensuring timely access to emergency services.
Year:
2017
Region / City:
European Union
Theme:
eCall, Emergency Communication, Vehicle Safety, Numbering Resources
Document Type:
Recommendation
Institution:
European Conference of Postal and Telecommunications Administrations (ECC)
Author:
European Conference of Postal and Telecommunications Administrations
Target Audience:
National authorities, car manufacturers, mobile operators, PSAPs
Period of Validity:
Ongoing
Approval Date:
22 November 2017
Modification Date:
None
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2017
Region / City:
European Union
Topic:
eCall Service, Emergency Communication
Document Type:
Recommendation
Organization / Institution:
European Conference of Postal and Telecommunications Administrations (ECC)
Author:
Not specified
Target Audience:
National authorities, mobile network operators, vehicle manufacturers
Validity Period:
From 22 November 2017
Approval Date:
22 November 2017
Amendment Date:
December 2020
Note:
Year
Subject:
Structural Special Inspections
Document Type:
Regulatory Text
Context:
Document outlining the requirements for structural special inspections for various materials including concrete, masonry, steel, cold-formed steel, post-installed anchors, aluminum, and wood.
Year:
2017
Region / City:
European Union
Topic:
eCall Service, Emergency Communication
Document Type:
Recommendation
Organization / Institution:
European Conference of Postal and Telecommunications Administrations (ECC)
Author:
Not specified
Target Audience:
National authorities, mobile network operators, vehicle manufacturers
Validity Period:
From 22 November 2017
Approval Date:
22 November 2017
Amendment Date:
December 2020
Year:
2021
Region / City:
Kranj, Slovenia
Topic:
NG eCall Interoperability
Document Type:
Proposal
Organization / Institution:
ETSI
Author:
Bostjan Pintar
Target Audience:
ETSI Members, Technical Experts
Period of Action:
2022-02-01 to 2023-03-31
Approval Status:
Approved by Ref. Body MSG
Date of Approval:
2021-06-03
Last Updated:
2021-11-09
Budget:
20,500 EUR
Number of Supporting ETSI Members:
4
Objectives:
Enhancement of interoperability tests for NG eCall
Standards Considered:
ETSI TS 103 683, ETSI TS 123 167, ETSI TS 124 229, ETSI TS 103 479, CEN TS 17249-1 to -6
Consequences if Not Agreed:
Potential issues in interoperability, affecting road safety
Deliverables:
ETSI TS 103 683 V2.1.1, CEN EN 15722:2020, CEN EN 16062:2021, among others
Resources:
35,500 EUR
Travel Budget:
2,500 EUR
Year:
2022
Region / City:
Europe
Theme:
Emergency communication systems, vehicle safety
Document Type:
ECC Report
Organization:
Electronic Communications Committee (ECC)
Author:
N/A
Target Audience:
Regulatory bodies, vehicle manufacturers, telecommunications providers
Period of Validity:
N/A
Approval Date:
7 June 2022
Date of Changes:
N/A
Year:
2017
Region / City:
European Union
Topic:
eCall Service, Emergency Communication
Document Type:
Recommendation
Organization / Institution:
European Conference of Postal and Telecommunications Administrations (ECC)
Author:
Not specified
Target Audience:
National authorities, mobile network operators, vehicle manufacturers
Validity Period:
From 22 November 2017
Approval Date:
22 November 2017
Amendment Date:
December 2020
Year:
2023
Region / City:
United States
Subject:
Pharmaceutical Regulatory Guidance
Document Type:
Guidance
Organization / Institution:
FDA
Author:
FDA
Target Audience:
Industry stakeholders, Sponsors, Applicants
Effective Period:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Note:
Contextual Description
Year:
2023
Region / City:
Global
Topic:
Biopharmaceutical studies, bioavailability, bioequivalence
Document Type:
Regulatory Guidance
Agency / Institution:
FDA, EMA
Author:
Not specified
Target Audience:
Industry professionals in pharmaceuticals
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Amendments:
Not specified
Note:
Year
Year:
2026
Region / City:
Global
Topic:
Clinical Efficacy Studies
Document Type:
Guidance
Author:
FDA
Target Audience:
Industry professionals in pharmaceuticals
Action Period:
Ongoing
Approval Date:
N/A
Modification Date:
N/A
Description:
Regulatory guidance on the structure and numbering of templates in eCTD submissions, with a focus on the proper organization and presentation of efficacy studies in pharmaceutical documentation.
Year:
2026
Region / city:
USA, Canada
Topic:
Active substance evaluation
Document Type:
Regulatory document
Organization:
Regulatory Authority (PMRA, EPA)
Author:
Applicant
Target Audience:
Regulatory authorities
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Changes:
Not specified
Year:
2020
Region / City:
Web meeting
Subject:
Minutes of the 21st WG NaN Meeting
Type of document:
Meeting minutes
Author:
Andrew Burns
Target audience:
Delegates representing CEPT administrations, ETSI, NTT, ECO
Period of validity:
15-17 December 2020
Date of approval:
15 December 2020
Date of amendments:
N/A
Year:
2018
Region / city:
The Hague, The Netherlands
Subject:
Meeting Report – PT FNI, Copenhagen
Source:
Chairman / Francesco Bernabei
Source e-mail:
[email protected]
Date of the document:
01 February 2018
Note:
Action items
Target audience:
PT FNI members
Action period:
2018
Context:
Report of the 36th PT FNI meeting, including discussions on the development of numbering strategies, work progress on number assignment, and preparations for upcoming conferences.
Year:
2025
Region / City:
International
Topic:
Document numbering system
Document Type:
Guideline
Organization / Institution:
ICCAT Secretariat
Author:
ICCAT Secretariat
Target Audience:
Delegations of CPCs
Period of validity:
2025
Approval Date:
N/A
Amendment Date:
N/A
Year:
2014
Region / City:
United States
Theme:
Fast Track Designation, Drug Development
Document Type:
Guidance
Organ / Institution:
FDA (Food and Drug Administration)
Author:
FDA
Target Audience:
Drug Sponsors, Pharmaceutical Industry
Period of Validity:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Year:
2018
Region / City:
United States
Topic:
Regulatory Guidance, Clinical Trials, Investigational Product
Document Type:
Regulatory Guidance
Organization / Institution:
FDA
Author:
FDA
Target Audience:
Industry Professionals, Investigators, Clinical Research Teams
Period of Validity:
N/A
Approval Date:
N/A
Date of Changes:
N/A
Year:
2001
Region / city:
N/A
Subject:
Pharmacokinetics, Drug Development
Document type:
Regulatory guidance
Author:
N/A
Target audience:
Industry professionals, pharmaceutical companies
Period of validity:
N/A
Approval date:
N/A
Date of amendments:
N/A
Year:
2022
Region / city:
Global
Topic:
Safety Data, Drug Exposure, Clinical Trials
Document Type:
Regulatory Guidance
Organization:
International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH)
Author:
Unknown
Target Audience:
Pharmaceutical Industry Professionals, Regulatory Authorities
Effective Period:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Note:
Year