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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
Dissemination and Confidentiality under REACH Regulation Dissemination and Confidentiality under REACH Regulation Dissemination and Confidentiality under REACH Regulation (2,165.2k)
Dissemination and Confidentiality under the REACH Regulation Release date October 2019 1 Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358 9 686180 |...
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29/10/19
Recommendations - introduction Recommendations - introduction Recommendations to registrants
All REACH registrants are encouraged to proactively update and review their information so as to improve the quality of their registration dossiers. The following...
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24/05/19
How to improve your dossier - evaluation How to improve your dossier - evaluation How to improve your dossier
Recommendations to registrants from evaluation
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04/12/18
How to change your substance identifier - regulations link How to change your substance identifier - regulations link How to change your substance identifier
See also under the Regulations section Substance identification
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13/11/18
News Keep your registration up to date, 6 November 2018 Special e-News, 6 November 2018 More information on dossier evaluation processes available, 18 October 2018 Data on...
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07/11/18
Latest news on REACH 2018 Latest news on REACH 2018 REACH 2018
Latest news on REACH 2018 Keep your registration up to date, 6 November ECHA increases visibility of authority activities, 15 October Member registrants will start receiving...
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06/11/18
Registration statistics - technical notes Registration statistics - technical notes Technical notes
Substance phase-in/non phase-in status and NONS allocation At the registration level phase-in/non phase-in status is derived by the status indicated by the company in the...
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23/10/18
How to improve your dossier - dqa - related document How to improve your dossier - dqa - related document Dossier quality assistant
Supporting material Video tutorial on how to use Validation assistant in IUCLID [YouTube] [EN] High level summary of all DQA rules [PDF] [EN] Download the latest version of...
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15/10/18
REACH 2018 Phase tabs REACH 2018 Phase tabs Assess hazard and risk
1. Know your portfolio 2. Find your co-registrants 3. Get organised with your co-registrants 4. Assess hazard and risk 5. Prepare your registration as a IUCLID dossier 6....
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03/10/18
Registration numbers granted to 32 515 REACH 2018 registrations Registration numbers granted to 32 515 REACH 2018 registrations Registration numbers granted to 32 515 REACH 2018 registrations
true News release 9999 false ECHA/NR/18/46 Registration numbers have been granted to 32 515 dossiers out of the 33 363 dossiers that were submitted by the final REACH...
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10/09/18
REACH 2018 - Find your co-registrants REACH 2018 - Find your co-registrants Find your co-registrants
Obligation to work together with your co-registrants All co-registrants for the same substance are part of a cooperation group called a substance information exchange forum...
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10/08/18
10 years REACH registration 10 years REACH registration 10 years REACH registration
10 years of REACH registration For 10 years, chemicals companies have assessed the risks of their chemicals used in Europe and sent that information to ECHA according to the...
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01/06/18
Registration dossiers for the 2018 Deadline Registration dossiers for the 2018 Deadline Registration dossiers for the 2018 Deadline (398.3k)
# Registrations % # Substances Registrations in Joint Submissions 26 582 97% 9 079 Lead 6 782 26% 6,501 Member 19 800 74% 4,858 Individual Registrations under REACH ...
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30/05/18
Under REACH, there is no obligation to register substances in amounts below one tonne a year. To further encourage innovation, substances used in scientific research and...
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23/05/18
News Simpler IUCLID Cloud now available to all REACH registrants, 15 May 2018 Watch a webinar: Guided dossier preparation in IUCLID Cloud, 14 February 2018 IUCLID Cloud now...
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15/05/18
Guidance for identification and naming of substances under REACH and CLP Guidance for identification and naming of substances under REACH and CLP Guidance for identification and naming of substances under REACH and CLP (1,639.4k)
Guidance for identification and naming of substances under REACH and CLP Version 2.1 - May 2017 3 G U I D A N C E Guidance for identification and naming of ...
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09/05/18
News REACH-IT closed for maintenance 4-5 June 2018 REACH-IT open 24/7 as of 16 March Enhanced completeness check delivers its first results, 15 February 2017 REACH 2018:...
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09/05/18
Benefit from a faster processing of your REACH dossier Benefit from a faster processing of your REACH dossier Benefit from a faster processing of your REACH dossier
true News release 9999 false ECHA/NR/18/14 Submit your REACH 2018 registration dossier before the end of March and receive ECHA’s decision on your registration within three...
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16/03/18
Support Letter template for data-sharing and joint submission negotiations [.docx] Help for registrants in exceptional situations - DCG solutions News Guidance on data...
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15/03/18
Registration statistics - overview of all countries Registration statistics - overview of all countries Registration statistics - overview of all countries (91.1k)
Registration Statistics # Registrations # Substances Registrations in Joint Submissions 50 500 9 497 Lead 10 056 N/A Member 40 444 N/A Individual Registrations...
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20/02/18
Helping registrants in exceptional cases Helping registrants in exceptional cases Helping registrants in exceptional cases
true News release 9999 false ECHA/NR/18/06 Companies facing exceptional situations that are likely to prevent them from registering on time should inform ECHA ahead of the...
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20/02/18
300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals 300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals 300 people gather in Helsinki for last minute advice ahead of the final registration deadline for chemicals
true Press release 2 false ECHA/PR/18/02 The European Chemicals Agency will host over 300 participants from industry, academia and authorities from all over the world for its...
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02/02/18
Non-EU Countries - Kosovo Non-EU Countries - Kosovo Non-EU/EEA countries
Kosovo Ministry of Environment and Spatial Planning Leaflet (AL) Leaflet (SR) Leaflet (EN) This designation is without prejudice to positions on status and is in line with...
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18/12/17
Toolkit for promoting the registration deadline Toolkit for promoting the registration deadline Toolkit for promoting the registration deadline
Does your organisation interact with manufacturers and importers of chemicals who need to register by 31 May 2018? Or, with users of chemicals who need to make sure their uses...
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07/12/17
Webinar: IUCLID Cloud - Best practice for service providers and SMEs Webinar: IUCLID Cloud - Best practice for service providers and SMEs Webinar: IUCLID Cloud - Best practice for service providers and SMEs
20171129020000 Chemical Watch Online Free webinar 15:00 - 16:00 Helsinki time (EET, GMT +2) aimed at consultants working with SMEs. Webinar: IUCLID Cloud - Best practice for...
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20/11/17
Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) Guidance in a nutshell - Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) (415.0k)
G U I D A N C E I N A N U T S H E L L Scientific Research and Development (SR&D), Product and Process Orientated Research and Development (PPORD) The document aims...
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19/10/17
Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) Guidance on Scientific Research and Development (SR&D) and Product and Process Oriented Research and Development (PPORD) (620.6k)
G U I D A NC E Guidance on Scientific Research and Development (SR&D) and Product and Process Orientated Research and Development (PPORD) Version 2.1 October 2017...
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19/10/17
reach2018 Denmark reach2018 Denmark member states
Denmark Miljø- og Fødevareministeriet, Miljøstyrelsen REACH Registering
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18/10/17
Consultants use case ECHA Cloud Services Cooperation goals • Prepare and submit registration dossier to ECHA • Be prepared for update submissions • Have an...
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09/10/17
Requesting an alternative chemical name in mixtures-Links Requesting an alternative chemical name in mixtures-Links Requesting a review of a decision on the use of an alternative chemical name
Related MB/17/2011: Decision Amending Decision MB/17/2008 establishing remedies for reviewing a partial or full rejection of a confidentiality request pursuant to Article 118(3)...
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19/09/17
REACH 2018 events navi REACH 2018 events navi events
February 2017 | March 2017 | April 2017 | May 2017 June 2017 | July 2017 | August 2017 | September 2017 | October 2017 | November 2017 | January 2018
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31/08/17
Form for describing the manufacturing process of UVCB substances 1 (2) August 2017 Annankatu 18, P.O. Box 400, FI-00121 Helsinki, Finland | Tel. +358...
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25/08/17
[Document title] 3 (4) Internal/Restricted/Confidential XX/xx dd Month yyyy Form for describing the manufacturing process of UVCB substances 1...
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25/08/17
Related documents under qsar models Related documents under qsar models QSAR models
Related Guidance on information requirements and chemical safety assessment, R.6 QSAR and grouping of chemicals
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17/08/17
Related Practical guide on how to use alternatives to animal testing [PDF] [EN]
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17/08/17
PPORD - related documents PPORD - related documents PPORD
Related Manual: How to prepare registration and submit a PPORD dossier notification Template for reporting justification for the request for extension [DOC] [EN]
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10/08/17
REACH 2018 - Upcoming REACH 2018 - Upcoming Know your portfolio
Support Contact your national REACH helpdesk or the ECHA helpdesk Form on the manufacturing process of UVCB substances [PDF] [Word file] News Last push to raise awareness about...
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10/08/17
Guidance in a nutshell Registration data and dossier handling Guidance in a nutshell Registration data and dossier handling Guidance in a nutshell Registration data and dossier handling (731.5k)
G U I D A N C E I N A N U T S H E L L Registration The document aims to explain in simple terms the registration obligations and briefly summarises the parent...
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05/07/17
Guidance on the Application of the CLP Criteria Guidance on the Application of the CLP Criteria Guidance on the Application of the CLP Criteria (13,658.2k)
Guidance on the Application of the CLP Criteria Version 5.0 – July 2017 1 G U I D A N C E Guidance on the Application of the CLP Criteria ...
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03/07/17
REACH 2018 Submit your registration dossier 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the European Chemicals Agency, to assist you in...
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31/05/17
REACH 2018 Prepare your registration as a IUCLID dossier 1 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the European Chemicals Agency, to...
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31/05/17
REACH 2018 Assess hazards and risks of your chemicals 1 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the European Chemicals Agency, to...
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31/05/17
REACH 2018 Get organised with your co-registrants – SIEF management and data sharing 1 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the...
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31/05/17
REACH 2018 Find your co-registrants and prepare to register jointly 1 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the European Chemicals...
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31/05/17
REACH 2018 Know your portfolio and start preparing now 1 2 Purpose of this presentation This presentation, with notes, was prepared by ECHA, the European Chemicals Agency, to...
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31/05/17

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