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Recommendations - information requirements Recommendations - information requirements Standard information requirements
Under REACH, standard information requirements are those that are required as a minimum to meet your registration obligations, and they depend directly on how much of a...
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31/07/20
Information on manual verification at completeness check Information on manual verification at completeness check Information on manual verification at completeness check (659.3k)
24 July 2020 1 Information on manual verification at completeness check ECHA performs a completeness check on each incoming registration to ensure that the ...
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30/07/20
How to improve your dossier - webinars table How to improve your dossier - webinars table Related webinars
Webinar related to dossier quality Content Date Substance identity issues covered in the screening campaign Concentration ranges Compositions with no constituents No...
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14/07/20
Legislation - REACH Regulation Legislation - REACH Regulation Legislation
REACH Regulation Consolidated version of the REACH Regulation The consolidated version of the Regulation (EC) No 1907/2006 of the European Parliament and of the Council on the...
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14/07/20
What information you need to submit What information you need to submit What you need to submit
As a registrant of a substance, you need to compile all the required information in a registration dossier, which has two main components: A technical dossier is always required...
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10/06/20
Submitting your registration dossier Submitting your registration dossier 6. Submitting your registration dossier
If you have prepared your registration dossier in IUCLID, you need to submit it to ECHA through REACH-IT. REACH-IT is the central IT system for companies to securely submit,...
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10/06/20
Strategy for gathering your data main Strategy for gathering your data main Strategy for gathering your data
There are four steps in the process of data gathering before registering a substance. Agree with your co-registrants how to divide the work or whether to outsource some, or all...
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10/06/20
Practical considerations before testing main Practical considerations before testing main Practical considerations before testing
Typically, tests are contracted out as a package. This has the advantage of being performed by experts in the most time-efficient manner and according to the required quality...
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10/06/20
In vitro methods main In vitro methods main In vitro methods
A test performed in vitro ("in the glass") means that it is done outside of a living organism and it usually involves isolated tissues, organs or cells. You can use in vitro...
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10/06/20
Intro: How to get organised for dossier updates Intro: How to get organised for dossier updates 7. How to get organised for dossier updates
The registration dossier has to reflect the current knowledge on how your substance can be used safely at production sites and by users throughout the supply chain. This...
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10/06/20
Do I reach the one tonne a year threshold? Do I reach the one tonne a year threshold? Do I reach the one tonne a year threshold?
If you manufacture or import a substance in amounts less than one tonne a year, you do not need to register the substance. If you reach or exceed this threshold, your tonnage...
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10/06/20
To register a substance in the 10 to 100 tonnage band, you need to provide information specified in Column 1 of REACH Annexes VII and VIII, comprising certain physicochemical...
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10/06/20
To register a substance in the 1 to 10 tonnage band, you need to provide information specified in Column 1 of REACH Annex VII, including certain physicochemical data,...
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10/06/20
How to create your registration dossier with the IUCLID Cloud How to create your registration dossier with the IUCLID Cloud How to create your registration dossier with IUCLID cloud
If you only have a few substances to manage, you can take advantage of the IUCLID Cloud to create your dossiers in the IUCLID format. To use the service, you will need an ECHA...
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10/06/20
how to avoid unnecessary animal testing main 1 how to avoid unnecessary animal testing main 1 How to avoid unnecessary testing on animals
Under REACH, testing on vertebrate animals (e.g. rats, other mammals or fish) can only be used as a last resort to fulfil information requirements for registration. There are...
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10/06/20
From submission to decision From submission to decision From submission to decision
Your dossier will go through the following steps after submission: 1. Business rules check The business rules check makes sure that your dossier can be processed by ECHA. For...
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10/06/20
Finding your co-registrants Finding your co-registrants 2. Finding your co-registrants
You will need to share data and register your substance jointly with other companies. In practice, this means that you need to: Submit an inquiry via REACH-IT to ask ECHA if you...
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10/06/20
Adaptations to standard information requirements Adaptations to standard information requirements Adaptations to the standard information requirements
Claiming an “adaptation” means that it is possible to omit a test based on certain general rules or specific rules that apply for just one information requirement. General rules...
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10/06/20
Collecting information on uses main Collecting information on uses main Collecting information on uses
In your registration dossier you also have to report / provide information on how your substance is used in your supply chain. To retrieve such information you can use many...
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10/06/20
Creating your registration dossier Creating your registration dossier 5. Creating your registration dossier
After you have compiled all the information on your substance necessary for fulfilling the REACH requirements, you need to document your findings in a registration dossier. The...
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10/06/20
what info you need top text what info you need top text 4. What information you need
The minimum data requirements for registration of your substance are specified in Annexes VI - X of REACH. The legal requirements (standard information requirements) are...
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10/06/20
What you need to consider for your business What you need to consider for your business What you need to consider for your business
Demonstrating the safe use of your substance in a registration dossier requires a significant investment of time, money and expertise. You will need to have dialogue and,...
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10/06/20
Does my substance need to be registered? Does my substance need to be registered? Does my substance need to be registered?
Once you know the identity of your substance, you need to see if your substance needs to be registered or if it is exempt from registration. On ECHA’s website you can check if...
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10/06/20
Do I need to register? Do I need to register? Do I need to register?
You need to determine whether it is you who needs to register a substance or another actor in your supply chain. 1. What is your identity as a registrant? You can only...
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10/06/20
Support - Registration Support - Registration Registration phases
In a registration you show that the substance you deal with is handled safely throughout the supply chain, ensuring that human health and the environment are protected. You...
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10/06/20
Substance registration Substance registration Registration
Companies are responsible for collecting information on the properties and uses of the substances they manufacture or import above one tonne a year. They also have to assess the...
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03/06/20
Understanding REACH Understanding REACH Understanding REACH
REACH is a regulation of the European Union, adopted to improve the protection of human health and the environment from the risks that can be posed by chemicals, while enhancing...
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03/06/20
How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers (4,419.8k)
How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers Release date April 2020 2 P.O. Box 400,...
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13/05/20
How to prepare an inquiry dossier How to prepare an inquiry dossier How to prepare an inquiry dossier (2,106.8k)
How to prepare an inquiry dossier 2 How to prepare an inquiry dossier Version 5.0 P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180...
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04/05/20
REACH-IT - registration process - Q&A links REACH-IT - registration process - Q&A links Registration Process
Questions and Answers Pre-registration Inquiry Registration Joint submission NONS
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20/04/20
These Dos and Don'ts can help make negotiations successful. Dos Don'ts Before the negotiations ✓ Establish and maintain clear contact details, if possible a functional...
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12/03/20
What is IUCLID What is IUCLID What is IUCLID?
IUCLID is a software to record, store, maintain and exchange data on intrinsic and hazard properties of chemical substances. ECHA co-develops the software with the OECD. Under...
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12/03/20
SMEs and consultants:See also SMEs and consultants:See also SME-consultant cooperation
See also under the Legislation section Registration
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11/03/20
Reduced information requirements - see also regulation Reduced information requirements - see also regulation Reduced information requirements
See also under the Legislation section Registration
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06/03/20
Practical advise for submitting jointly Practical advise for submitting jointly Practical advice for sharing data
The following elements must be part of the data-sharing agreement: Data itemisation The existing registrant must provide information on the specific data to be shared. This...
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06/03/20
Working together with your co-registrants Working together with your co-registrants 3. Get organised with your co-registrants
REACH requires existing registrants and potential registrants to make every effort to reach an agreement on sharing data. The legislation also requires that the costs of sharing...
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06/03/20
REACH Nanomaterial registrations - message REACH Nanomaterial registrations - message Registered substances
The result of the search ‘Substance has nanoform’ returns all factsheets containing data related to nanomaterials. However, this does not mean that a registration covering...
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25/02/20
Recommendations - substance id Recommendations - substance id Substance identification
REACH requires all registrants to provide sufficient information to identify the substance they manufacture or import. There must be only one registration for each substance, so...
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25/02/20
Recommendations - cnl Recommendations - cnl Classification and labelling
Classification and labelling is crucial for ensuring a high level of protection of health and the environment, as well as for the free movement of substances, mixtures and...
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24/02/20
Recommendations - substance ev - panels Recommendations - substance ev - panels Decision under substance evaluation
Substance evaluation is carried out by the EU Member States. It aims to clarify concerns related to the safe use of a substance. The evaluating competent authority may request...
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24/02/20
Recommendations - dossier ev - panels Recommendations - dossier ev - panels Decision under dossier evaluation
If ECHA considers that your registration dossier is not compliant with the information required for your substance at the tonnage band registered, it will issue a decision. This...
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24/02/20
Recommendations - exposure and risk - panels Recommendations - exposure and risk - panels Exposure assessment and risk characterisation
You need to carry out exposure assessment and risk characterisation for substances registered at or above 10 tonnes per year, if they are classified as dangerous or as having...
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24/02/20
Recommendations - adaptions panels Recommendations - adaptions panels Adaptations
An adaptation to a standard information requirement means that instead of performing a test, you provide a justification that is either based on general rules or on specific...
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21/02/20
Related Guidance on information requirements and chemical safety assessment, R.6 QSAR and grouping of chemicals The Read-across assessment framework [PDF] [EN] Human health:...
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18/02/20
Recommendations - registration Recommendations - registration Registration
You are responsible for collecting information on the tonnages, properties and uses of the substances you manufacture or import in quantities of more than one tonne a year. You...
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18/02/20
Revommendations to registrants - general- toptext Revommendations to registrants - general- toptext General recommendations
These general recommendations highlight ECHA’s key messages for keeping your registration data in order and improving it proactively. Update regularly You are responsible for...
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18/02/20
Registration - obligations -links Registration - obligations -links 1. Your registration obligations
Support Practical examples – REACH registration How to cooperate for REACH registration – best practice for SMEs and consultants
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18/02/20
Prepare your registration as a IUCLID dossier - practical examples Prepare your registration as a IUCLID dossier - practical examples Practical examples – REACH registration
5 Prepare your registration as a IUCLID dossier How to protect your confidential business information [PDF] These video tutorials highlight different aspects in preparing...
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18/02/20
Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures
Related Commission Directive (EU) 2019/1831 of 24 October 2019 establishing a fifth list of indicative occupational exposure limit values Commission Directive (EU) 2017/164 of...
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08/01/20
Diss disabled 20191202 Diss disabled 20191202 Designated National Authority
Due to IT maintenance activities, some substance tables are temporarily disabled. We will resume the service as soon as possible. ECHA apologises for any inconvenience caused. ...
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02/12/19

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