№ lp_1_2_11256
File format: docx
Character count: 16306
File size: 433 KB
The document outlines the guidelines for setting the shelf-life of biocidal products during the authorisation process, ensuring clarity and consistency between different official documents and providing a framework for data requirements for applications.
Year:
2022
Region / City:
EU
Subject:
Biocides, Product Authorisation
Document Type:
Agreement
Organization:
Coordination Group
Author:
Coordination Group Members
Target Audience:
EU Member States, Biocidal Product Applicants
Period of validity:
N/A
Approval Date:
22 September 2022
Amendment Date:
N/A
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The product description is provided for reference. Actual content and formatting may differ slightly.
Year:
2024
Region / city:
Global
Theme:
Nanotechnology in food packaging
Document type:
Review article
Institution:
Not specified
Author:
Not specified
Target audience:
Researchers, food industry professionals
Period of validity:
Not specified
Approval date:
Not specified
Modification date:
Not specified
Year:
2022
Region / city:
European Union
Subject:
Biocidal products family, Regulation (EU) No 528/2012
Document type:
Guidance note
Institution:
European Commission
Period of validity:
N/A
Approval date:
N/A
Amendment date:
N/A
Contextual description:
A guidance note outlining the procedure for addressing biocidal product families under Regulation (EU) No 528/2012, with a focus on ongoing and past product authorizations.
Year:
2021
Region / City:
Great Britain
Topic:
Biocidal Products Regulation, Biocidal Products
Document Type:
Consultation Document
Organization:
Health and Safety Executive (HSE)
Author:
Health and Safety Executive (HSE)
Target Audience:
Businesses, stakeholders in the biocidal products industry
Period of Application:
From Autumn 2023
Approval Date:
Not specified
Date of Changes:
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:
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
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:
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:
2025
Region / city:
Brussels
Topic:
Biocidal products, Regulations, European Union
Document type:
Meeting minutes
Organization:
European Commission
Author:
European Commission
Target audience:
Competent Authorities, EU Member States
Period of validity:
N/A
Approval date:
N/A
Date of changes:
N/A
Summary:
Meeting minutes documenting discussions on the adoption of regulations related to biocidal products, including delegated acts, changes to authorizations, and coordination group reports.
Year:
2026
Region / City:
Helsinki, Finland
Topic:
Biocidal products, Human hygiene
Document type:
Repository document
Organization / Institution:
European Chemicals Agency
Author:
European Chemicals Agency
Target audience:
Professionals in biocide regulation
Validity period:
January 2026
Approval date:
January 2026
Modification date:
N/A
Year:
2020
Region / City:
European Union
Topic:
Biocidal Products, Chemical Regulation
Document Type:
Explanatory Memorandum
Agency / Organization:
European Commission
Author:
European Commission
Target Audience:
European Union Member States, Regulatory Authorities, Biocidal Product Stakeholders
Period of Validity:
Indefinite
Approval Date:
2020
Date of Amendments:
N/A
Year:
2019
Region / city:
Ireland
Topic:
Investment company, liquidation
Document type:
Consultation Paper
Institution:
Central Bank of Ireland
Author:
Central Bank of Ireland
Target audience:
Investment companies, financial institutions
Period of validity:
Indefinite until revocation
Date of approval:
July 2019
Date of amendments:
N/A
Purpose:
Outline of the appeal process for reviewable decisions
Jurisdiction:
South Australia
Scheme:
South Australian Restrictive Practices Authorisation scheme
Legal basis:
Disability Inclusion Act 2018 (Part 6A, ss. 23L, 23N, 23O, 23P, 23Y, 23Z)
Regulations:
Disability Inclusion (Restrictive Practices – NDIS) Regulations 2021, s. 14
Document type:
Administrative procedure
Responsible unit:
Restrictive Practices Unit
Decision-makers:
Authorised Program Officer; Senior Authorising Officer; South Australian Civil and Administrative Tribunal
Scope:
Appeals of reviewable decisions relating to restrictive practices
Target audience:
RPU staff, people with disability, family members, NDIS service providers
Appeal timeframe:
30 days from original decision, with possible extension
Review bodies:
Senior Authorising Officer; South Australian Civil and Administrative Tribunal
Source type:
Government administrative procedure governing appeals and reviews of restrictive practice authorisation decisions within the South Australian NDIS regulatory framework.
Note:
Year
Theme:
Special Religious Education, Child Protection
Document Type:
Authorisation Letter
Organisation / Institution:
Department of Education
Target Audience:
Approved Providers, School Coordinators
Year:
2024
Region / City:
Malta
Topic:
ICT Third-Party Service Providers
Document Type:
Regulatory Form
Organization / Institution:
Malta Financial Services Authority (MFSA)
Author:
Malta Financial Services Authority (MFSA)
Target Audience:
Financial entities applying for authorisation from MFSA
Effective Period:
Not specified
Approval Date:
Not specified
Amendment Date:
Not specified
Year:
2003
Jurisdiction:
Victoria, Australia
Document type:
Application form / Regulatory form
Regulation:
Cemeteries and Crematoria Regulations 2025, Regulation 30
Issuing authority:
Victorian Government
Related legislation:
Births, Deaths and Marriages Registration Act 1996; Coroners Act 2008; Privacy and Data Protection Act 2014; Public Records Act 1973
Purpose:
Authorisation of cremation for deceased persons
Attachments required:
Notice of death, Certificate of registered medical practitioner, Coroner’s order, notice of still-birth (if applicable)
Penalties:
False statements punishable under section 132 of the Cemeteries and Crematoria Act 2003
Applicant type:
Natural person or corporate body
Cremation details:
Name of crematorium, date of cremation, place and type of interment
Contact information:
Applicant and funeral director details, including address, telephone, and email
Year:
2003
Region / City:
Victoria, Australia
Theme:
Cemeteries and Crematoria Regulations
Document Type:
Form
Author:
Victoria State Government
Target Audience:
Individuals arranging for interment of bodily remains
Effective Period:
N/A
Approval Date:
N/A
Amendment Date:
2025