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true Czech Republic BPR competent authority Ministry of Health of the Czech Republic Palackeho namesti 4 CZ - 128 01 Prague 2 Telephone: +420 267 082 305 Fax: +420 267 082 228 Email: biocidy (at)...
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06/04/22
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general
The SCEDs in chesar format are included the 'Use map' chesar file (see above). Further supporting information on SCEDs is available in the explanatory document below. Solvents, Surfactants,...
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05/04/22
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general
Technical problems with ECHA’s public chemicals database Following some technical fixes, and an initial round of improvements, data is once again available on the ECHA website. We are monitoring...
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04/04/22
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QA1763
E. Confidentiality, Invoicing
I do not wish to keep my confidentiality claim anymore, can I get a refund from ECHA of the fee I paid for the claim? The fee paid for the confidentiality claim is to cover our work assessing your...
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31/03/22
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QA1762
E. Confidentiality, Invoicing
I claimed confidentiality but did not receive an invoice? What is the reason for it? If confidentiality is claimed on information covered by REACH Article 119(2), normally a fee is levied to cover...
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31/03/22
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QA1770
D. Confidentiality, SDS
Can I claim confidentiality on the Chemical Safety Report (CSR)? We currently do not publish the CSR itself. A confidentiality claim in section 13, where the CSR is attached does not cover the CSR...
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31/03/22
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QA1766
C. Confidentiality, Study summaries
How do I know whether the test material reference substance is flagged confidential? Check that the flag appears in any of the following locations: a. There is a confidentiality flag on the IUPAC...
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31/03/22
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QA1765
C. Confidentiality, Study summaries
In our read-across data, if we would like to claim the source endpoint(s) confidential, do we also need to place a CBI on the target endpoint? You may claim the source endpoint(s) confidential...
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31/03/22
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QA1767
C. Confidentiality, Study summaries
What information is published as part of the test material? From the study document Contents of the field Dissemination rule 'Test material information' the link itself is published to enable...
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31/03/22
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QA1759
B. Confidentiality, Dossier creation
We have confidential information in the attached documents in IUCLID. How do we claim them confidential? Under REACH, only information entered into a IUCLID field is published. Attachments are not...
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31/03/22
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QA1769
B. Confidentiality, Dossier creation
Where will the Third-Party Representative’s (TPR) identity be made visible? If you have correctly assigned a TPR, you can verify its visibility on the following pages in REACH-IT. You will see the...
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31/03/22
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QA1896
B. Confidentiality, Dossier creation
How can I hide my identity from the public? To hide the company’s identity from the public, you need to claim it by setting the confidentiality flag in Section 1.1 of the IUCLID registration...
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31/03/22
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QA1768
B. Confidentiality, Dossier creation
What can I do to hide my identity both from the public and also from the co-registrants? It is possible to hide your identity both from the public and also from your co-registrants throughout the...
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31/03/22
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QA1758
B. Confidentiality, Dossier creation
I have just submitted a dossier but forgot to include the confidentiality claim(s). What do I do? Please contact us via our contact form, as soon as you notice that the information has not been...
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31/03/22
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QA1771
B. Confidentiality, Dossier creation
How can I claim confidentiality on the IUPAC name of my substance? Regarding confidentiality claims on the IUPAC name we distinguish four scenarios: Claim type Substance is classified in...
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31/03/22
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QA1756
B. Confidentiality, Dossier creation
How can I successfully claim confidentiality? You can follow the below steps before uploading your registration dossier to REACH-IT, to ensure that your confidentiality claim is successful: ...
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31/03/22
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QA1761
A. Confidentiality, general
My confidentiality claim was accepted however the information is published. Why is it published? ECHA combines data per substance from all regulatory activities, therefore the information may be...
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31/03/22
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QA1760
A. Confidentiality, general
Can my claim be accepted if the claimed information is in the public domain? Please see our explanatory document on How to protect you confidential business information, section 1. false 1760
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31/03/22
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general
Dissemination Platform 4.8.0 (9 March 2022) REACH Registered Substance Factsheets The IUCLID 6.6 dossier format is now supported, so such dossiers can be processed and published. Dossiers received...
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31/03/22
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general
View online CLP Ad hoc consultation on harmonised classification and labelling of glyphosate The proposal for the harmonised classification and labelling of glyphosate (EC 213-997-4, CAS...
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30/03/22
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general
Volume III Human health Part A: Information Requirements Reference name: Guidance on the BPR: Volume III Human Health (Part A) Description: This Guidance describes the information requirements for...
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29/03/22
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Volume I Identity/physico-chemical properties/analytical methodology Parts A+B+C: Information Requirements, Assessment and Evaluation Reference name: Guidance on the BPR: Volume I...
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29/03/22
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general
1 An application/review report is received in terms of Article 64(1) of REACH when ECHA has received the application fee. 2 One opinion refers to a compiled version of the final opinions of RAC and...
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29/03/22
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general
<script src="//my.visme.co/visme-embed.js"></script><div class="visme_d" data-title="OEL process" data-url="vd7yjonz-oel-process" data-w="575" data-h="400" data-domain="my"></div>
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29/03/22
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Volume IV Environment Part A: Information Requirements Reference name: Guidance on the BPR: Volume IV Environment (Part A) Description: This Guidance describes the information requirements for...
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29/03/22
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Volume II Efficacy Part A: Information Requirements Reference name: Guidance on the BPR: Volume II Efficacy (Part A) Description: This Guidance describes the information requirements for active...
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29/03/22
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QA1299
C. Joint submission management, lead registrant
How can the lead registrant decrease the Joint Submission’s tonnage band? Step 1 Before decreasing the Joint Submission tonnage band, the Lead Registrant needs to make sure that all members of the...
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25/03/22
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general
Disclaimer: These examples illustrate different practices of how applications for authorisation have been prepared. They are neither endorsed by, nor should they be considered as binding on, the...
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25/03/22
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general
The Ad hoc Working Group on the Assessment of Residue Transfer to Food (ARTFood) will support the Biocidal Products Committee and its Working Groups (especially the Working Group on Human Health)...
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23/03/22
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View online Highlights from March RAC and SEAC meetings The Committee for Risk Assessment (RAC) adopted its opinion supporting Norway’s proposal to restrict Dechlorane Plus. The Committee for...
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23/03/22
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general
Candidate list Registration Authorisation Restrictions Evaluation CLH Biocides ATD Company size
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21/03/22
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general
The Forum is composed of one appointed member from each EU Member State, Norway, Iceland and Liechtenstein. The members are appointed for a period of three years (renewable). There is also the...
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21/03/22
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general
This table contains all the court cases closed with a ruling to which ECHA has been a party. Interested parties can easily refer to decisions that may be relevant to them within the scope of ECHA's...
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21/03/22
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View online Mapping of potentially harmful chemicals on target to meet 2027 goal In 2021, we continued mapping registered substances to identify those requiring risk management or more data to...
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18/03/22
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ECHA has created a mapping tool of all registered substances called the chemical universe in which each substance is assigned to a pool that indicates the regulatory actions already initiated or...
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15/03/22
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general
In Annex V to the BPR the biocidal products are classified into 22 biocidal product-types, grouped in four main areas. As a result of excluding biocidal products used as preservatives for food and...
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14/03/22
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../file-system/small/txt
QA1550
A. Dissemination BPR, General (2)
What information is available for biocides? The following information is available in the “Information on chemicals” section for Biocides: The list of biocidal active substances for which an...
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14/03/22
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../file-system/small/txt
QA1626
B. Dissemination BPR, Search (2)
How can I ensure that the information published related to the BPR relies solely on Biocides data? The search results available in the “Search for chemicals” entry available in the ECHA homepage...
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14/03/22
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QA1625
B. Dissemination BPR, Search (2)
How is information derived from more than one SPC handled? When more than one SPC is provided in the same biocidal product authorisation, i.e., different language versions, the “Information on...
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14/03/22
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../file-system/small/txt
QA1622
B. Dissemination BPR, Search (2)
What can I expect using the search functionalities for biocidal products? The extended search functionalities allows you to search for products based on trade names, uses of the product (target...
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14/03/22
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../file-system/small/txt
QA1556
B. Dissemination BPR, Search (2)
I cannot find information from an application on ECHA’s website. Why? The most common reasons are: Data from active substance or biocidal product applications must be available in R4BP 3, i.e., new...
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14/03/22
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../file-system/small/txt
QA1555
A. Dissemination BPR, General (2)
Certain information from my published approval/authorisation is incorrect/missing. What shall I do? When you notice that certain published information from your active substance/authorisation is...
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14/03/22
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../file-system/small/txt
QA1554
A. Dissemination BPR, General (2)
How can I ensure that confidential information will not be published? During the approval / authorisation process for an active substance or a biocidal product, the applicant has to provide...
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14/03/22
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../file-system/small/txt
QA1553
A. Dissemination BPR, General (2)
When will the information from my application be published on ECHA’s website? Information on biocidal product authorisations will be published in the “Information on chemicals” section on ECHA’s...
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14/03/22
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../file-system/small/txt
QA1552
A. Dissemination BPR, General (2)
How does ECHA guarantee the reliability of Biocides data publicly available? The biocides data available in the “Information on chemicals” section on the ECHA’s website originates from the...
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14/03/22
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QA1551
A. Dissemination BPR, General (2)
What information is available in the biocidal product factsheet? The biocidal product factsheet contains detailed information on the biocidal product’s authorisation as available in R4BP 3. The...
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14/03/22
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general
The Ad hoc Working Group Microorganisms will focus on matters related to biocides containing microorganisms (microbial active substances). It will support the BPC and its Working Groups during the...
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14/03/22
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general
Find here the annual Declarations of Interest of the members
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11/03/22
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general
View online REACH Substance evaluation: decisions soon sent to registrants Member States will finalise the 2021 substance evaluation on 17 March 2022. ECHA will send the finalised draft decisions...
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09/03/22
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general
Due to planned maintenance, commenting forms will be unavailable on Thursday March 10th, 18.30-22.00.
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08/03/22
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