№ lp_1_2_45061
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This document provides guidance to Member States for reporting under the recast Drinking Water Directive 2020/2184/EC.
Date:
20 September 2023
Note:
Region / City
Theme:
Drinking Water, Water Quality
Document Type:
Guidance Document
Agency / Institution:
European Commission, Directorate-General for Environment
Target Audience:
Member States, European Commission, European Environment Agency (EEA)
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2013
Region / City:
London
Subject:
Train Slot Recasting and Dispute Resolution
Document Type:
Legal Response
Institution:
Network Rail Infrastructure Limited
Author:
Not specified
Target Audience:
Freightliner Heavy Haul Limited, Network Rail, Timetable Panel
Period of Validity:
December 2013 timetable
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2021
Region / City:
EU
Topic:
Zero-emission buildings, energy performance
Document Type:
Technical report
Organization / Institution:
European Union
Author:
Johann Zirngibl, Jana Bendzalova
Target Audience:
Policymakers, researchers, energy professionals
Action Period:
2021
Approval Date:
15.12.2021
Amendment Date:
None
Year:
2025
Region / city:
Australia
Subject:
Airworthiness directive
Document type:
Regulatory directive
Issuing authority:
Civil Aviation Safety Authority (CASA)
Author:
David Punshon
Target audience:
Aviation maintenance personnel, aircraft operators
Effective date:
01 June 2025
Amendments:
Amendment 6
Compliance time:
12 calendar months for Requirement 1, 100 hours TIS or 12 months for Requirement 2, 20 years TIS for Requirement 3
Background:
Initial issue date: 1 February 1996
Year:
2021
Region / City:
European Union
Topic:
Cross-border marketing of EU AIFs
Document type:
Notification letter
Author:
European Commission
Target audience:
AIFMs, regulatory bodies, financial institutions
Period of validity:
Not specified
Approval date:
Not specified
Amendment date:
Not specified
Year:
2025
Region / City:
Oregon
Topic:
Health Care, Advance Directives
Document Type:
Legal Form
Author:
Oregon Health Authority
Target Audience:
Residents of Oregon, those preparing Advance Directives
Period of Validity:
Not specified
Date of Approval:
Not specified
Date of Changes:
July 15, 2025
Year:
2017
Note:
Region / City
Subject:
Civil Aviation Safety
Document Type:
Compliance Statement
Year:
2026
Region / City:
United States
Topic:
Data Validation, Eligibility Documentation
Document Type:
Directive
Agency / Institution:
State Government
Author:
Unknown
Target Audience:
State agencies, program administrators, and relevant stakeholders
Period of Validity:
Not specified
Approval Date:
Not specified
Date of Amendments:
Not specified
Year:
2016
Region / city:
Victoria, Australia
Topic:
Advance care directive, medical treatment, personal health
Document type:
Instructional guide
Organization:
Health.vic
Author:
Unknown
Target audience:
Adults creating an advance care directive
Validity period:
Indefinite
Approval date:
Unknown
Amendment date:
Unknown
Document title:
QD83 – Global Supplier Quality Directive
Edition:
2018
Document type:
Supplier acknowledgement and acceptance form
Issuing organization:
ZF Friedrichshafen AG
Applicable standard:
QD83
Related documents:
QD83-2018 Sanctioned Interpretations
Scope of applicability:
All current and future supplies to ZF Friedrichshafen AG and affiliated companies within the ZF Group
Target audience:
Suppliers of ZF Friedrichshafen AG
Legal reference:
German Stock Law §§ 15
Replacement clause:
Replaces all previous agreements on ZF Supplier Quality Directives
Exclusions:
Specific quality assurance agreements remain unaffected
Geographic scope:
Global
Language:
English
Year:
2016
Region / City:
European Union
Theme:
Financial Regulation, Supervisory Reporting
Document Type:
Instructional Guide
Organization / Institution:
European Union
Author:
European Commission
Target Audience:
Third-Country Branches, Financial Institutions, Regulatory Authorities
Period of Validity:
Ongoing
Date of Approval:
Not specified
Date of Modifications:
Not specified
Document type:
Supervisory reporting instructions
Legal basis:
Directive 2013/36/EU, Article 48k(1)
Jurisdiction:
European Union
Scope:
Financial and regulatory reporting by third-country branches
Applicable entities:
Third-country branches (Class 1 and Class 2)
Reporting framework:
Implementing Regulation XXXX (ITS on TCBs reporting)
Templates covered:
E 01.01, E 01.02, E 02.00, E 03.01, E 03.02, E 04.01, E 04.02, E 05.01, E 05.02, E 06.01, E 06.02, E 07.01, E 07.02, E 08.01, E 08.02, E 09.01, E 09.02, E 10.00
Accounting standards:
IFRS as adopted under Regulation (EC) No 1606/2002 or applicable national GAAP
Subject matter:
Assets and liabilities, off-balance sheet items, internal transactions, capital endowment, liquidity coverage, and deposit protection arrangements
Source type:
Regulatory guidance document
Year:
2025
Region / City:
Malaysia
Topic:
Export control regulations for advanced AI chips
Document type:
Guideline
Organization:
Strategic Trade Secretariat, Ministry of Investment, Trade and Industry (MITI)
Author:
Strategic Trade Secretariat
Target Audience:
Exporters, manufacturers, regulatory bodies
Effective Period:
Ongoing from 2025
Approval Date:
2025
Amendment Date:
N/A
Year:
2025
Region / City:
KwaZulu-Natal
Topic:
Court Online System Implementation
Document Type:
Draft Directive
Institution:
KwaZulu-Natal Division of the High Court
Author:
Office of the Chief Justice
Target Audience:
Legal practitioners, litigants
Period of validity:
From 1 April 2025
Approval Date:
Not specified
Date of amendments:
Not specified
Note:
Year
PART 1:
Information on the AIFM or internally managed AIF
PART 2:
Information on the AIFs to be marketed in the host Member State
Document type:
Regulatory guidance
Regulatory framework:
Directive 2001/20/EC; Regulation (EU) No 536/2014
Subject:
Transition of clinical trials from CTD to CTR
Applicable documents:
Protocol; Investigator’s Brochure; Investigational Medicinal Product Dossier
Regulatory authorities involved:
National Competent Authorities; Ethics Committees
Geographical scope:
European Union Member States
Related systems:
CTIS; EudraCT
Intended user:
Sponsor of multinational clinical trials
Referenced guidance:
EudraLex Volume 10; CTCG Best Practice Guide; European Commission Q&A
Document status:
Informational requirements for transition applications
Scope of changes addressed:
Non-substantial changes; harmonised and consolidated documents; auxiliary medicinal products; IMPD-Q submissions
Year:
2023
Region / City:
European Union
Topic:
Clinical Trials, Medical Regulation
Document Type:
Cover Letter
Organization:
European Commission
Author:
European Commission
Target Audience:
Pharmaceutical Companies, Clinical Trial Sponsors
Action Period:
Transition of Clinical Trials from Directive 2001/20/EC to Regulation (EU) No 536/2014
Approval Date:
N/A
Amendment Date:
N/A
Place of preparation:
Amsterdam
Regulatory framework:
Directive 2001/83/EC
Article:
Article 10(c)
Committee:
Committee for Medicinal Products for Human Use (CHMP)
Associated committee:
Pharmacovigilance Risk Assessment Committee (PRAC)
Document type:
Regulatory assessment report template
Application type:
Informed consent marketing authorisation application
Scope:
Medicinal products for human use
Responsible authority:
European Medicines Agency
Assessment procedure:
Joint CHMP and PRAC assessment
Peer review:
Not foreseen
Applicable dossier modules:
Module 1 with references to Modules 2–5
Related process:
Marketing Authorisation Application
Communication channel:
Eudralink
Intended users:
CHMP and PRAC Rapporteurs, National Competent Authorities
Document structure:
Administrative, scientific, clinical, and pharmacovigilance sections
Template status:
Draft with guidance notes