№ lp_1_2_29917
File format: docx
Character count: 47813
File size: 740 KB
This document provides regulatory guidelines and technical recommendations for the authorisation of in situ biocidal products, addressing the complexities of managing product approvals for substances generated in situ.
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
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:
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:
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:
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:
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.