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../file-system/small/txt ../file-system/small/txt Art 95 list download
art_95_list_en.pdf 22/04/2024 art_95_list_en.xlsx
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22/04/24
Art. 95 list, List of Active Substances and Suppliers Art. 95 list, List of Active Substances and Suppliers art_95_list_en.xlsx (329 KBk)
Art. 95 list, List of Active Substances and Suppliers
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22/04/24
../file-system/small/txt ../file-system/small/txt Approved suppliers - links
See also Questions and Answers on Active substance suppliers Questions and Answers on Data sharing and related disputes under BPR Data sharing List of active substances and suppliers (Article 95...
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09/04/24
Art. 95 list (List of Active Substances and Suppliers) Art. 95 list (List of Active Substances and Suppliers) art_95_list_en.pdf (2.3 MBk)
Art. 95 list (List of Active Substances and Suppliers)
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20/03/24
../file-system/small/txt ../file-system/small/txt Understanding BPR - external links
See also Getting started with EU chemicals legislation European Commission - Biocides Biocidal Products Directive (Directive 98/8/EC) Biocides Relevant Document Links R4BP 3 user manuals Guidance...
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15/03/24
Approval of an active substance Prepare your IUCLID dossier. Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘AS-APP – Approval of active substance' to launch the application ‘wizard' which...
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08/02/24
../file-system/small/txt ../file-system/small/txt Active substances toptext
Make sure that you have everything you need before making your application. The Biocides Submission Manual (BSM) ‘Application instructions: How to submit an application for Active Substance'. The...
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08/02/24
../file-system/small/txt ../file-system/small/txt Submit applications - IT-Tools
IT-Tools IUCLID R4BP 3
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07/02/24
Related Submit a dossier - R4BP 3 BPR Coordination Group
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01/06/23
../file-system/small/txt ../file-system/small/txt Active substance action plan link
Active substance action plan Guidelines for assessing confidentiality claims [EN][PDF] MSCA Assessment Reports submission plan [EN][PDF]
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14/04/23
* See "BPC opinions on Approval of active substances" on the page of the Biocidal Products Committee.
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15/02/23
../file-system/small/txt ../file-system/small/txt Biocidal Products Regulation
Biocidal Products Regulation Consolidated version of the Biocidal Products Regulation The consolidated version of the Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22...
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13/01/23
Related ECHA's open invitation page Notification procedure List of active substances and suppliers Q&As on In-situ generated active substances CA documents on in-situ generated active substances WG...
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02/09/22
Manuals and guidance Biocides Submission Manuals Guidance on biocides legislation Practical Guides on BPR ECHA accounts and EU Login Q&A Supporting documents
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01/09/22
../file-system/small/txt ../file-system/small/txt Understanding BPR
The Biocidal Products Regulation (BPR, Regulation (EU) 528/2012) concerns the placing on the market and use of biocidal products, which are used to protect humans, animals, materials or articles...
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08/06/22
See also PBT expert group Harmonised classification and labelling Biocidal Products Committee Risk Assessment Committee Union authorisation National authorisation
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20/04/22
See a problem or have feedback?
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08/04/22
See a problem or have feedback?
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08/04/22
Practical guide on Biocidal Products Regulation
Approval of active substance Practical guide on Biocidal Products Regulation Approval of active substance pg_on_bpr_1_approval_active_substances_en.pdf (394 KBk)
Practical guide on Biocidal Products Regulation Approval of active substance
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21/12/21
BPC opinion on a request according to Article 75(1)(g) under BPR BPC opinion on a request according to Article 75(1)(g) under BPR bpc_opinion_comparative-assessment_ar_en.pdf (390 KBk)
BPC opinion on a request according to Article 75(1)(g) under BPR
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15/11/21
Manual on submitting information in the consultation on potential candidates for substitution under BPR Manual on submitting information in the consultation on potential candidates for substitution under BPR bpr_cons_instructions_en.pdf (183 KBk)
Manual on submitting information in the consultation on potential candidates for substitution under BPR
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15/11/21
../file-system/small/txt ../file-system/small/txt Biocides maintenance II
Due to a technical problem, which is being fixed, certain substance/product-type combinations are currently displayed with an inaccurate status. See the correct status for those...
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31/05/21
../file-system/small/txt ../file-system/small/txt Content pages - Subscribe
Follow us Read ECHA Weekly news Subscribe to our news
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08/04/21
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04/01/21
Related Commission CA paper [DOC] List of active substances and suppliers List of compliant notifications [PDF]
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03/07/20
../file-system/small/txt ../file-system/small/txt Article 93 transitional measure
Article 93 of the BPR provides for a derogation to its Article 17(1) - the biocidal product authorisation requirement - in the shape of transitional measures. These transitional measures can...
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03/07/20
Disclaimer Authentic version: Only the Article 95 list published on this website in PDF format is deemed authentic. The XLS version is made available as a courtesy in order to facilitate companies...
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26/05/20
I have read and I accept the legal notice . Download the list of active substances and suppliers Download the list of active substances and suppliers [PDF][EN] 25 May 2020 Download the list of...
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26/05/20
See also ECHA contact forms Article 95 LoA template [DOC][EN] Approval of active substances Q&A on Active substances suppliers Request for correction of entries on the Art.95 list [DOC][EN]
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15/05/20
Active substances meeting the following exclusion criteria should normally not be approved: carcinogens, mutagens and reprotoxic substances categories 1A or 1B according to the CLP Regulation...
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02/04/20
Related Submission of information in the consultation on potential candidates for substitution under the Biocidal Products Regulation [PDF][EN]
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02/04/20
Consultations Consultation on potential candidates for substitution Consultation on derogation to the exclusion criteria
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12/03/20
The closed consultations on the derogations to the exclusion criteria as laid down in Article 5(2) of the BPR are listed in the table below. Current consultations
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04/03/20
How to submit a contribution to the consultation? The consultation lasts for 60 days. Interested third parties wishing to contribute to the consultation must submit the contribution and relevant...
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04/03/20
../file-system/small/txt ../file-system/small/txt BPC sidebar - link
About us Biocidal Products Committee Working groups
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15/04/19
Related Biocidal Active Substances List of notifications [PDF]
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11/04/19
../file-system/small/txt ../file-system/small/txt BPR - upcoming dadlines - footnotes
* The comprehensive list of the applicable deadline for each of the compliant notification is given in List of notifications ** Article 3(2) RPR applications can only be made by the successful...
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11/04/19
../file-system/small/txt ../file-system/small/txt BPR-upcoming deadlines-toptext
The following deadlines are listed to help companies to comply with their obligations under the Biocidal Products Regulation (BPR) and the Review Programme Regulation (RPR). AS = active substance...
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12/02/19
Active substances need to be approved before an authorisation for a biocidal product containing them can be granted. The active substances are first assessed by an evaluating Member State...
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19/12/18
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28/09/18
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28/09/18
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28/09/18
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28/09/18
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28/09/18
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28/09/18
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28/09/18
Biocidal Products Committee (BPC)
Opinion on a request according to Article 75(1)(g) of Regulation (EU) No 528/2012 on
Sulfuryl fluoride PT 8 and 18
Assessment of new information on global warming potential
ECHA/BPC/073/2015 Biocidal Products Committee (BPC) Opinion on a request according to Article 75(1)(g) of Regulation (EU) No 528/2012 on Sulfuryl fluoride PT 8 and 18 Assessment of new information on global warming potential ECHA/BPC/073/2015 bpc_opinion_art_175_1_g_sulfuryl_fluoride_en.pdf (111 KBk)
Biocidal Products Committee (BPC) Opinion on a request according to Article 75(1)(g) of Regulation (EU) No 528/2012 on Sulfuryl fluoride PT 8 and 18 Assessment of new information on global warming...
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28/09/18
Opinion of the Biocidal Products committee Opinion of the Biocidal Products committee bpc_opinion_heiq_ags-20_en.pdf (113 KBk)
Opinion of the Biocidal Products committee
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28/09/18
Opinion of the Biocidal Products committee Opinion of the Biocidal Products committee bpc_opinion_polymeric_binder_art_75_1_en.pdf (151 KBk)
Opinion of the Biocidal Products committee
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28/09/18
The proposed combinations that appear in the table below are considered eligible for inclusion in the Review Programme and they result from either "successful declarations of interest",...
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25/06/18
*Note for the open invitations resulting from redefinition, this invitation concerns only substances covered by the name here and not the name to which the substances are redefined (Article 14 of...
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25/06/18
These deadlines in Biocidal Products Regulation (BPR) and the Review Programme Regulation (RPR) have passed. AS = active substance PT = product type AS/PT = active substance/ product-type...
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13/06/18
../file-system/small/txt ../file-system/small/txt Existing active substance top text
The Review Programme is the name commonly used for the work programme for the examination of existing biocidal active substances contained in biocidal products. The programme was set up by the...
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20/12/17
European Commission includes approved active substances in the Union list of approved active substances (formerly Annex I of Directive 98/8/EC). Companies wishing to get an authorisation for a...
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13/10/17
Related R4BP 3
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05/09/17
Related Successful declarations of interest Withdrawals of all participants Redefinitions How to submit a notification in the Review Programme
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15/08/17
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11/08/17
../file-system/small/txt ../file-system/small/txt Submit applications - Related links
Related Appeals Data sharing ECHA Helpdesk National helpdesks
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10/08/17
Related Guidance on data sharing Guidance on active substance suppliers Guidance on Information requirements
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04/08/17
Related Prepare a dossier - IUCLID Submit a dossier - R4BP 3 Biocides Submission Manuals
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03/08/17
../file-system/small/txt ../file-system/small/txt BPR - Annex I amendment - links
Related Simplified authorisation Biocidal Product Committee
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03/08/17
Related Treated articles: allowed active substances Review Programme Regulation (EU) No 1062/2014 How to submit a notification in the Review Programme
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03/08/17
Related Practical Guide chapter on approval of active substance [PDF] [EN]
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03/08/17
../file-system/small/txt ../file-system/small/txt Understanding BPR - related links
Related Approval of active substances Authorisation of biocidal products Technical equivalence Active substance suppliers Data sharing
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03/08/17
Follow up your applications Important – make a note of your submission number. You will need it for further reference. Important - check your tasks and messages in R4BP 3 regularly. They can...
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14/06/17
Notification of substances that benefitted from the derogation for food
and feed Notification of substances that benefitted from the derogation for food and feed notification_requirements_food_n_feed_en.pdf (188 KBk)
Notification of substances that benefitted from the derogation for food and feed
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24/01/17
List of substances deadlines List of substances deadlines list_substances_deadline_en.pdf (260 KBk)
List of substances deadlines
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24/01/17
The evaluation process starts when an application for amendment of Annex I to the BPR is considered to be valid by the evaluating competent authority. The evaluating competent authority has 180...
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16/12/16
Companies will submit applications through R4BP 3. A IUCLID file is required. This graph shows an overview of dossier submission for the amendment of Annex I. Steps Dossier submission proceeds in...
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16/12/16
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13/09/16
../file-system/small/txt ../file-system/small/txt In situ generated active substances
Biocidal active substances are called in situ generated active substances if they are generated from one or more precursors at the place of use. The approval of such substance requires evaluation...
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04/07/16
In situ active substance/precursor-combination open for notification In situ active substance/precursor-combination open for notification biocides_substances_redefined_identity_en.pdf (206 KBk)
In situ active substance/precursor-combination open for notification
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19/01/16
Related links Guidance on information requirements Product-types How to submit a notification in the Review Program (Role of participant or for inclusion of a new Active substance)
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13/01/16
../file-system/small/txt ../file-system/small/txt New active substance
Companies have to apply for approval of an active substance by submitting a dossier to ECHA. After the validation check has been performed by ECHA, the evaluating competent authority carries out a...
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17/12/15
../file-system/small/txt ../file-system/small/txt BPR - Annex I amendment
Active substances that can be contained in biocidal products eligible for simplified authorisation procedure Annex I of the Biocidal Products Regulation (BPR) lists initially active substances...
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17/12/15
Suggested template letter of access for Article 95 of the BPR (complete substance dossier) Suggested template letter of access for Article 95 of the BPR (complete substance dossier) template_letter_access_article_95_bpr_en.docx (50 KBk)
Suggested template letter of access for Article 95 of the BPR (complete substance dossier)
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04/08/15
Companies will apply for inclusion on the list of active substance suppliers through R4BP 3. This graph shows an overview of the application procedure for inclusion on the list of active substance...
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23/03/15
An application for the approval of an active substance (inclusion in the Union list of approved active substances) or for the inclusion in Annex I of the BPR (with the exclusion of category 7) can...
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06/03/15
Active substances already in the review programme (Annex II part 1) and active substances which will be added to the programme after the submission of a compliant notification will be evaluated as...
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06/03/15
See also Annex III to the Review Programme Regulation - Time limits [PDF]
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06/03/15
Application for approval or inclusion in Annex I Dossier submission Evaluation process
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05/03/15
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04/03/15
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04/03/15
The notification process to take over the role of participant or to include an active substance/product-type in the Review Programme has the following steps: A notifier (prospective...
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23/12/14
../file-system/small/txt ../file-system/small/txt Active substances - support
Support Small or Medium-sized Enterprises (SMEs)
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03/12/14
../file-system/small/txt ../file-system/small/txt Submit applications - Legislation
Legislation Legislation Biocidal Products Regulation explained Commission Implementing Regulation (EU) No 564/2013 (Fee Regulation)
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02/12/14
active_substance_suppliers_application.jpg active_substance_suppliers_application.jpg active_substance_suppliers_application (154 KBk)
active_substance_suppliers_application.jpg
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02/12/14
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30/10/14
The assessment reports can be found in the list of Biocidal Active Substances.
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02/05/14
The Biocidal Products Committee has issued the following opinions on questions that have arisen from the operation of the Biocidal Products Regulation (BPR) relating to technical guidance or risks...
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30/04/14
The Biocidal Products Committee has issued the following opinions on active substance approval:
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28/04/14
../file-system/small/txt ../file-system/small/txt BPR-research-development-content1
Any tests and experiments carried out for research and development purposes using unauthorised biocidal products and their (not approved) active substances must be recorded and may require...
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06/03/14
Regulations Implementing Regulation (EU) No 564/2013 (Fee Regulation)
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21/02/14
Regulations Biocidal Products Regulation Regulation (EU) 528/2012 Implementing Regulation (EU) No 88/2014
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21/02/14
Regulations Biocidal Products Regulation Regulation (EU) 528/2012 See also Biocidal Product Committee Simplified authorisation
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20/02/14
annex_i_submission_en.png annex_i_submission_en.png annex_i_submission_en (7 KBk)
annex_i_submission_en.png
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20/02/14
annex_i_evaluation_process_en.png annex_i_evaluation_process_en.png annex_i_evaluation_process_en (6 KBk)
annex_i_evaluation_process_en.png
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20/02/14
Steps Dossier submission proceeds in several steps. Each step needs to be completed before the application can move to the next step. It is important that the applicant makes sure that all...
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27/11/13
This graph shows an overview of the dossier evaluation process
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25/11/13
This graph shows an overview of the dossier submission process.
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25/11/13