№ lp_1_2_22057
File format: docx
Character count: 1760
File size: 70 KB
The document provides a system for numbering and revising ICCAT documents based on specific codes for different types of sessions and panels, and explains the process for revisions and the reduction of printed copies for sustainability purposes.
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
Price: 8 / 10 USD
The file will be delivered to the email address provided at checkout within 12 hours.
The file will be delivered to the email address provided at checkout within 12 hours.
Don’t have cryptocurrency yet?
You can still complete your purchase in a few minutes:- Buy Crypto in a trusted app (Coinbase, Kraken, Cash App or any similar service).
- In the app, tap Send.
- Select network, paste our wallet address.
- Send the exact amount shown above.
The final amount may vary slightly depending on the payment method.
The file will be sent to the email address provided at checkout within 24 hours.
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
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:
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
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:
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
Year:
N/A
Region / City:
N/A
Subject:
Pharmaceutical Documentation, eCTD
Document Type:
Regulatory Guidance
Organization / Institution:
FDA
Author:
N/A
Target Audience:
Pharmaceutical Industry
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
Organization:
International Commission for the Conservation of the Atlantic Tunas
Submitting party:
European Union
Type of document:
Draft recommendation with explanatory note
Subject:
Record of authorized large-scale fishing vessels
Geographic scope:
ICCAT Convention area
Vessel length threshold:
20 metres overall or greater
Reporting obligations:
Annual reporting of active vessels and imports of ICCAT species
Addressees:
Contracting Parties and Cooperating Non-Contracting Parties
Implementation date:
Entry into force of the CMM
First reporting deadline:
15 September 2026 for vessels active in 2025
Language:
English
Organization:
International Commission for the Conservation of Atlantic Tunas (ICCAT)
Secretariat:
ICCAT Secretariat
Year:
2024–2025
Geographic scope:
Atlantic Ocean and adjacent seas
Thematic areas:
Fisheries management; Conservation measures; Reporting requirements; Fleet capacity; Bycatch mitigation
Species concerned:
Tropical tunas; North Atlantic swordfish; Mediterranean albacore; Bluefin tuna; Skipjack tuna; Mobulid rays; Sharks; Seabirds
Document type:
Compilation of repealed measures and technical proposals
Legal instruments referenced:
Recommendations and Resolutions of ICCAT
Status of measures:
Repealed and replaced by recommendations adopted in 2024
Related bodies:
SCRS; Panels 1, 2 and 4
Timeframe referenced:
Measures up to 2024; future considerations through 2026–2027
Year:
2025
Region / City:
Global
Subject:
Tropical tuna fishing, Mediterranean swordfish, compliance and management
Document type:
Report
Author:
ICCAT Secretariat
Target audience:
ICCAT Compliance Committee
Period of validity:
2024
Approval date:
2025
Date of amendments:
None
Year:
2024
Region / city:
International
Subject:
Fisheries management, conservation
Document type:
Recommendation, Resolution
Institution:
ICCAT Secretariat
Author:
ICCAT Secretariat
Target audience:
ICCAT Contracting Parties
Period of validity:
2024
Approval date:
2024
Amendment date:
2024
Year:
2025
Region / city:
Eastern Atlantic, Mediterranean
Topic:
Bluefin tuna management
Document Type:
Recommendation
Organization / Institution:
International Commission for the Conservation of Atlantic Tunas (ICCAT)
Author:
European Union
Target Audience:
Contracting Parties and Cooperating non-Contracting Parties, Entities or Fishing Entities
Period of validity:
2026-2028
Approval Date:
2025
Modification Date:
Not specified