№ lp_1_2_28527
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Character count: 4506
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This document is an application letter seeking a decision under Regulation 13/14/46 of the Railways (Interoperability) Regulations 2011 for a specific project in the UK rail sector.
Year:
2011
Region / City:
London
Topic:
Railways, Interoperability, Safety Regulations
Document Type:
Application Letter
Organization:
Department for Transport
Author:
PROJECT ENTITY
Target Audience:
Competent Authority, Rail Interoperability Team
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
N/A
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Date:
APRIL 2024
Duration:
2 Hours
Year:
2024
Region / City:
Kenya
Theme:
Environmental Sustainability
Document Type:
Examination Paper
Institution:
Riara School of International Relations & Diplomacy
Author:
Riara School of International Relations & Diplomacy
Target Audience:
University students
Period of Action:
January - April 2024
Approval Date:
April 2024
Date of Modifications:
Not specified
Year:
2023
Region / City:
European Union
Subject:
Biocidal Products Regulation (EU) No 528/2012
Document Type:
Report
Organization / Institution:
European Chemicals Agency (ECHA)
Author:
European Chemicals Agency (ECHA)
Period of Validity:
Ongoing, with updates from 2015 to 2023
Approval Date:
December 2023
Date of Last Changes:
December 2023
Year:
2024
Region / city:
Not specified
Topic:
Biocidal products
Document type:
Meeting minutes
Institution:
European Commission
Author:
Not specified
Target audience:
Competent Authorities of EU Member States
Period of validity:
Not specified
Approval date:
Not specified
Date of amendments:
Not specified
Context:
Meeting minutes of the 106th session of the Competent Authorities for the implementation of Regulation (EU) No 528/2012, discussing issues related to biocidal products and their regulation within the EU.
Year:
2024
Region / City:
European Union
Topic:
Biocidal Products, Legislation
Document Type:
Meeting Minutes
Organization / Institution:
European Commission
Author:
European Commission
Target Audience:
Competent Authorities of Member States
Period of validity:
26-27 September 2024
Approval Date:
27 September 2024
Date of amendments:
None
Contextual Description:
Minutes of a meeting of the representatives of Competent Authorities from Member States, discussing the implementation of Regulation (EU) No 528/2012 concerning biocidal products.
Year:
2015
Region / city:
European Union
Subject:
Management of product authorisation for in situ cases
Type of document:
Official guideline
Organization:
European Commission
Target audience:
Competent Authorities, applicants for biocidal product authorisation
Effective period:
Ongoing
Approval date:
23 June 2015
Year:
2023
Region / city:
Brussels
Subject:
Chemicals, Classification, and Labelling
Document Type:
Meeting Record
Organ / institution:
European Commission
Author:
Directorate-General for Environment, Directorate-General for Internal Market, Industry, Entrepreneurship and SMEs
Target audience:
Competent Authorities for REACH and CLP
Period of validity:
06/03/2024
Approval date:
06/03/2024
Date of changes:
N/A
Contextual description:
A record of the 50th meeting of the Competent Authorities for REACH and CLP, discussing updates on the Globally Harmonized System, ongoing work on new hazard classes, and the implementation of GHS revisions.
Year:
2023
Region / City:
European Union
Subject:
Biocidal products, Regulation (EU) No 528/2012, Union authorisation
Document Type:
Official Discussion Paper
Authoring Organization:
European Commission
Period of Validity:
Ongoing
Date of Approval:
N/A
Date of Last Revision:
N/A
Year:
2022
Region / City:
Europe
Topic:
Biocidal products
Document Type:
Agenda
Organization / Institution:
Competent Authorities for the implementation of Regulation (EU) No 528/2012
Author:
N/A
Target Audience:
Member States Competent Authorities
Period of Validity:
22-23 June 2022
Approval Date:
N/A
Date of Modifications:
N/A
Date:
28/04/2022
Region / City:
Brussels
Subject:
Polymers, Chemicals Strategy
Document Type:
Background Document
Organization:
European Commission, Directorate-General for Environment
Author:
European Commission
Target Audience:
REACH and CLP Competent Authorities, Environmental Experts
Period of Application:
May 2022
Approval Date:
28/04/2022
Year:
2017
Region / city:
European Union
Subject:
Implementing the concept of biocidal product family
Document type:
Guidance note
Author:
European Commission
Period of validity:
Ongoing
Approval date:
November 2014
Date of changes:
March 2017, July 2017
Keywords:
Biocidal product family, authorisation, regulation, EU, risk assessment, efficacy
Year:
1993
Region / City:
South Africa
Topic:
Occupational Health and Safety
Document Type:
Appointment Letter
Institution:
Employer
Author:
CEO
Target Audience:
Employee
Period of Validity:
Ongoing
Approval Date:
Not specified
Modification Date:
Not specified
Year:
2015
Region / city:
International
Topic:
Medical Device Regulation
Document Type:
Official Report
Organization / Institution:
International Medical Device Regulators Forum (IMDRF)
Author:
National Competent Authority Report Working Group
Target Audience:
Medical Device Regulators, Public Health Authorities
Period of validity:
Ongoing
Approval Date:
26 March 2015
Date of amendments:
None
Year:
2024
Region / city:
EU
Topic:
Biocidal products, PFAS substances, REACH Regulation
Document type:
Regulatory document
Organization / institution:
Competent Authorities of Member States
Author:
Not specified
Target audience:
Competent Authorities, stakeholders in biocidal products regulation
Period of validity:
Not specified
Approval date:
September 2024
Date of changes:
Not specified
Year:
2024
Region / city:
Great Britain
Topic:
Nuclear safety, radioactive material transport
Document type:
Technical assessment guide
Organization / institution:
Office for Nuclear Regulation (ONR)
Author:
Nuclear Safety Inspector
Target audience:
ONR inspectors, regulatory authorities
Period of validity:
Until August 2029
Approval date:
October 2024
Revision date:
August 2029