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Praktiline juhend. Kuidas esitada (Q)SAR-meetodeid?
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26/08/16
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Registration
Praxisanleitungen: Meldung von Daten mit dem (Q)SAR-Ansatz
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26/08/16
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Praktisk vejledning. Rapportering af (Q)SAR’er
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26/08/16
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Практическо ръководство: Как да докладваме (Q)SARs
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26/08/16
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Registration
Praktický průvodce: Jak oznamovat (Q)SAR
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26/08/16
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Registration
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24/08/16
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Registration
Related documents Guidance on information requirements and chemical safety assessment, R.4 Evaluation of available information (Chapter R4.4) and R.7 Endpoint specific guidance
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18/07/16
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Registration
Related IT tools REACH-IT IUCLID QSAR Toolbox
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18/07/16
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Registration
Support Use maps Downstream users
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18/07/16
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Registration
An important part of the SIEF work with your co-registrants is to compile information on uses, hazards and risks in order to demonstrate safe use of the substance. You will need to consider the...
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12/07/16
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Registration
Tips Make use of ECHA's Read–Across Assessment Framework to check the robustness of your read-across adaptation. Give a hypothesis-driven justification why the data from one substance can be used...
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12/07/16
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Registration
Tips Present a clear and detailed description of the results, the test conditions and the interpretation of the results. This is important if the study is used as a key study or as part of a weight...
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12/07/16
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Registration
Tips Use (Q)SARs for physicochemical properties and for some environmental toxicity and fate properties. Currently (Q)SARs are not suitable for complex toxicological properties, as they are not fit...
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12/07/16
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Registration
Structure-activity relationship (SAR) and quantitative structure-activity relationship (QSAR) models - collectively referred to as (Q)SARs - are mathematical models that can be used to predict the...
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12/07/16
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Registration
Tips A proper weight of evidence approach includes, as a minimum, two separate study records for the property - also when using textbook values. One single value from a secondary data source is not...
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12/07/16
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Registration
The weight of evidence approach means that you use a combination of information from several independent sources to give sufficient evidence to fulfil an information requirement. This approach is...
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12/07/16
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Registration
Tips Prepare a well-documented and valid scientific justification if you adapt the standard information requirements and submit it in your registration dossier. The approach you choose must deliver...
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12/07/16
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Registration
Practical guide 5:How to report (Q)SARs
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04/07/16
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Registration
REACH-IT – what you need to know
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30/06/16
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Find useful information in this short guide to help you get started in REACH-IT and have a quick overview of the system
discover_reach_it_en.pdf
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Find useful information in this short guide to help you get started in REACH-IT and have a quick overview of the system
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21/06/16
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Registration
Grouping of substances and read-across is one of the most commonly used alternative approaches for filling data gaps in registrations submitted under REACH. This approach uses relevant information...
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20/06/16
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Registration
Registering your substance Potential registrants of substances (at one tonne or more per year), are required to prepare and submit a registration dossier to ECHA. Please note that you need to keep...
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17/06/16
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Registration
Requesting a registration number for NONS A REACH registration number can be claimed for a substance with a recognised notification number under Directive 67/548/EEC (also called NONS). To get this...
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16/06/16
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Registration
11th Stakeholders' day - Presentation
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25/05/16
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11th Stakeholders' day - Presentation
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25/05/16
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ECHA's strategy to support registrants
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15/04/16
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Registration
ECHA’s REACH 2018
Roadmap
Progress Report
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12/04/16
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Decizia Consiliului de administrație nr. 14/2015
Public (document de referință MB/43/2014)
4 iunie 2015
DECIZIE DE MODIFICARE A DECIZIEI MB/D/29/2010 ASTFEL CUM A FOST MODIFICATĂ PRIN DECIZIA MB/21/2012 CU PRIVIRE LA CLASIFICAREA SERVICIILOR PENTRU CARE SE PERCEP DREPTURI
mb_decision_14_2015_ro.pdf
(92 KBk)
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Decizia Consiliului de administrație nr. 14/2015
Public (document de referință MB/43/2014)
4 iunie 2015
DECIZIE DE MODIFICARE A DECIZIEI MB/D/29/2010 ASTFEL CUM A FOST MODIFICATĂ PRIN DECIZIA...
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23/03/16
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Registration
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03/03/16
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Partners and networks
IRECTORS’ CONTACT GROUP
DCG3/7/AP3a
FIRST EDITION
WITH NOTE, JAN 2016
FAIR, TRANSPARENT AND NON-DISCRIMINATORY COST SHARING IN SIEFS
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05/02/16
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Registration
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23/11/15
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Registration
Companies manufacturing and importing the same substance have to register jointly. If the substances are not the same they should not register jointly. How can you decide when two substances are...
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10/11/15
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Registration
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20/10/15
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20/10/15
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20/10/15
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