№ lp_1_2_62533
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This guidance note provides a harmonised approach for the implementation of the biocidal product family concept within EU regulation, offering clarification on grouping products based on similar efficacy and risks.
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
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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:
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
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:
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:
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:
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
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