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Related List of product-types Similar conditions of use Comparative assessment CA documents on Biocidal product family concept Overview of Article 44 (5) requests
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16/04/24
../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
Authorisation of biocidal products Prepare your IUCLID dossier. Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘SA-APP – National authorisation - simplified procedure'. The application...
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08/02/24
../file-system/small/txt ../file-system/small/txt Simplified authorisations 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 Simplified...
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08/02/24
Getting started – pre-submission Prepare your SPC file. Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘UP-APP – Pre-submission for union authorisation' to launch the application ‘wizard',...
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08/02/24
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 Union Authorisation'....
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08/02/24
Notification for a product in a product family Create your SPC file from the authorised SPC of the reference family asset. From the ‘ASSETS' tab, search for the relevant national authorisation...
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07/02/24
../file-system/small/txt ../file-system/small/txt Submit applications - IT-Tools
IT-Tools IUCLID R4BP 3
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07/02/24
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 National Authorisation...
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07/02/24
Regulations Biocidal Products Regulation - Annex I Regulation (EU) 528/2012
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31/08/23
To meet the needs of companies and reduce their administrative burdens, the Same Biocidal Products Regulation (Regulation 414/2013, amended by Regulation 2016/1802) introduces the possibility to...
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07/06/23
The Biocidal Product Regulation defines the renewal of a national authorisation as "an application by or on behalf of an authorisation holder wishing to seek the renewal of a national authorisation...
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01/06/23
Related Submit a dossier - R4BP 3 BPR Coordination Group
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01/06/23
National authorisation Companies planning to sell their products in one EU Member State must apply for product authorisation in that country. To do so, they submit an application for national...
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01/06/23
../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
../file-system/small/txt ../file-system/small/txt Related Links BPR product family
Related Prepare a dossier – IUCLID Submit a dossier – R4BP 3 Biocides Submission Manuals CA documents on biocidal product families Practical Guides
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02/09/22
Related Prepare a dossier - IUCLID Submit a dossier - R4BP 3 Guidance on Information Requirements Biocides Submission Manual Nanomaterials and the Biocidal Products Regulation Biocidal product...
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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
Once the reference Member State Competent Authority (MSCA) has validated the application for the renewal of the national authorisation of a biocidal product (or a biocidal product family) granted...
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10/06/22
../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
../file-system/small/txt ../file-system/small/txt Authorisation of biocidal products
Related Bridging the endocrine disruptor assessment of biocidal non-active substances with REACH (agreed at 91st CA meeting) [PDF][EN] Guidelines for assessing confidentiality claims [EN][PDF]...
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12/04/22
../file-system/small/txt ../file-system/small/txt Biocidal products - need help
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08/04/22
Authorisation of biocidal products family Authorisation of biocidal products family Instructions_biocidal_product_family_overview_v2_en.pdf (1.4 MBk)
Authorisation of biocidal products family
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14/01/22
Authorisation of biocidal products family Authorisation of biocidal products family biocidal_product_family_overview_v2-1_en.xlsx (72 KBk)
Authorisation of biocidal products family
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14/01/22
Proposal to bridge the endocrine disruptor assessment of biocidal non-active substances with REACH screening and assessment Proposal to bridge the endocrine disruptor assessment of biocidal non-active substances with REACH screening and assessment ca-march21-Doc43_final_bridging_biocides_with _reach_en.pdf (346 KBk)
Proposal to bridge the endocrine disruptor assessment of biocidal non-active substances with REACH screening and assessment
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22/04/21
../file-system/small/txt ../file-system/small/txt Content pages - Subscribe
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08/04/21
Further information Authorisation of Biocidal Products Products types BPR Regulation Q&A Biocidal Products Regulation BPC opinions on Union authorisation
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15/04/19
../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
../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
Authorisation cancellation on request Log into R4BP 3. From the ‘ASSETS’ tab, search for the specific asset number by filling in some search criterion. Clicking on the asset number hyperlink in the...
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23/11/18
Classification of a change to a product authorisation Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘CC-APP – Classification of a change to a product authorisation' to launch the...
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23/11/18
Renewal of authorisation(s) (including authorisations subject to mutual recognition) Log into R4BP 3. From the ‘ASSETS' tab, search for the relevant national authorisation asset you wish to renew....
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23/11/18
Mutual recognition in sequence Draft your SPC file from the authorised SPC of the reference asset. Log into R4BP 3. You can launch your application in two different ways: From the ‘NEW APPLICATION'...
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23/11/18
Mutual recognition in parallel Draft your SPC file from the SPC of the reference case. Log into R4BP 3. You can launch your application in three different ways: During the submission of an...
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23/11/18
Authorisation of biocidal products Prepare your IUCLID dossier. From the ‘NEW APPLICATION' tab, select ‘NA-APP – Application for national authorisation' to launch the application ‘wizard', which...
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23/11/18
Inquire to share data for a biocidal product Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘IN-REB – Inquire to share data (for biocidal product)' and enter the reference number (the...
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23/11/18
Parallel trade Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘PP-APP – Parallel trade' and enter the reference numbers (the national authorisation asset number in the Member State of...
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23/11/18
Notification of experiment or test Prepare your IUCLID dossier. Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘ET-NOT – Notification of experiment or test' to launch the application...
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23/11/18
Notification of unexpected or adverse effect Log into R4BP 3. From the ‘ASSETS' tab, search for the relevant national authorisation asset for which you wish to notify unexpected or adverse effect.....
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23/11/18
Transfer of authorisation The owner of a national authorisation asset must first initiate a transfer process in R4BP 3, this is done in the ‘Delegation/ Nomination’ tab of the asset. Once the owner...
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23/11/18
Merge of product authorisation(s) in one product family Draft your SPC file from the authorised SPC of the reference asset. Log into R4BP 3. From the ‘NEW APPLICATION' tab, select ‘NA-MRG – Merge...
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23/11/18
Administrative change on request Draft your SPC file from the authorised SPC of the reference asset. Log into R4BP 3. From the ‘ASSETS' tab, search for the relevant national authorisation asset for...
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23/11/18
Minor and major change on request Prepare your IUCLID dossier. Log into R4BP 3. From the ‘ASSETS' tab, search for the relevant national authorisation asset for which you wish to request a change....
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23/11/18
Authorisation of the same biocidal product (pending and authorised) Create your SPC file from the authorised SPC of the reference family case or asset, using specific functionality in the SPC...
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22/11/18
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
Related R4BP 3
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05/09/17
../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 Information Requirements Biocidal Product Committee Substitution criteria
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04/08/17
../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