Search

Results for tag Registration
Most relevant Last modified
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...
Similar Results Similar Results
09/06/21
How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers How to prepare registration and PPORD dossiers (3,541.0k)
How to prepare registration and PPORD dossiers April 2021 How to prepare registration and PPORD dossiers Release date April 2021 2 P.O....
Similar Results Similar Results
28/04/21
Dissemination and Confidentiality under REACH Regulation Dissemination and Confidentiality under REACH Regulation Dissemination and Confidentiality under REACH Regulation (2,334.8k)
Dissemination and Confidentiality under the REACH Regulation Release date April 2021 1 P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 | echa.europa.eu ...
Similar Results Similar Results
28/04/21
How to prepare an inquiry dossier How to prepare an inquiry dossier How to prepare an inquiry dossier (2,366.6k)
How to prepare an inquiry dossier April 2021 How to prepare an inquiry dossier Release date April 2021 2 P.O. Box 400, FI-00121...
Similar Results Similar Results
28/04/21
Requesting an alternative chemical name in mixtures Requesting an alternative chemical name in mixtures Requesting an alternative chemical name in mixtures
Manufacturers, importers and downstream users based in the EU can submit a request for the use of an alternative chemical name to ECHA. It is not possible to appoint a ‘Third...
Similar Results Similar Results
08/03/21
PPORD PPORD PPORD
Summary If your substance is subject to product and process orientated research and development (PPORD), you can submit a PPORD notification to ECHA in order to be exempted from...
Similar Results Similar Results
04/03/21
Recommendations - information requirements Recommendations - information requirements Standard information requirements
To meet your registration obligations, you must fulfil the minimum standard information requirements set by REACH. These requirements depend on the volume of the substance you...
Similar Results Similar Results
04/03/21
Information on manual verification at completeness check Information on manual verification at completeness check Information on manual verification at completeness check (278.1k)
22 February 2021 1 Information on manual verification at completeness check ECHA performs a completeness check on each incoming registration to ensure that...
Similar Results Similar Results
01/03/21
Registration - support Registration - support Registration
See also under the Support section Registration Questions and Answers on Registration
Similar Results Similar Results
25/02/21
Recommendations - substance ev - related Recommendations - substance ev - related Substance evaluation decisions
Related Substance evaluation – CoRAP table Substance evaluation Evaluation process Practical guide on how to act in substance evaluation Community rolling action plan
Similar Results Similar Results
22/02/21
Recommendations - risk mgmt - related Recommendations - risk mgmt - related Classification and labelling
Related Understanding CLP C&L Inventory How to submit and update your C&L notification Implementing Regulation (EU) 2020/1435
Similar Results Similar Results
22/02/21
Recommendations - substance id - related Recommendations - substance id - related Substance identification
Related Substance identification process under REACH Substance identification – get started Guidance on substance identification How to prepare registrations for nanomaterials...
Similar Results Similar Results
22/02/21
Revommendations to registrants - general- related Revommendations to registrants - general- related General recommendations
Related Public activities coordination tool Substances of potential concern Examination of testing proposals Strategy for gathering your data Adaptations Good Laboratory...
Similar Results Similar Results
22/02/21
Recommendations - cnl box Recommendations - cnl box Recommendations to registrants
Classification and labelling
Similar Results Similar Results
22/02/21
Recommendations - registration Recommendations - registration Registration
If your company manufactures or imports substances in quantities of more than one tonne per year, you are responsible for compiling and submitting a registration dossier to...
Similar Results Similar Results
22/02/21
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...
Similar Results Similar Results
22/02/21
Recommendations - dossier ev - panels Recommendations - dossier ev - panels Dossier evaluation decisions
In dossier evaluation, ECHA checks if the information that you have submitted in your registration meets the requirements set in REACH for your substance and tonnage band. If...
Similar Results Similar Results
22/02/21
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. Your justification has to either be based on general...
Similar Results Similar Results
22/02/21
Annex III modification Annex III modification Annex III modification
Please note that Annex III has been modified by Regulation 2018/1881, modifying provisions in case of nanomaterials (Commission Regulation (EU) 2018/1881 of 3 December 2018...
Similar Results Similar Results
08/02/21
Diss 4.5 maintenance - registered substances Diss 4.5 maintenance - registered substances Registered substances
Please note: The REACH Registered substance portal was updated on 9th November 2020; the REACH registered factsheets were further updated on 21st December 2020. Details of the...
Similar Results Similar Results
18/01/21
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...
Similar Results Similar Results
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,...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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,...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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,...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
10/06/20
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...
Similar Results Similar Results
03/06/20
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
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
12/03/20
SMEs and consultants:See also SMEs and consultants:See also SME-consultant cooperation
See also under the Legislation section Registration
Similar Results Similar Results
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
Similar Results Similar Results
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...
Similar Results Similar Results
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...
Similar Results Similar Results
06/03/20
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:...
Similar Results Similar Results
18/02/20

Categories Display