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How can I update the information in my pre-registration?

You can modify all information, except for the substance identity (see also QA 1142) and the legal entity assigned to that pre-registration. You can modify:

  • Contact information (both internal contact of the owner and possible third party representative).
  • The remarks field for the pre-SIEF if needed.
  • Similar substance fields.
How do I delete/deactivate my pre-registration?

A pre-registration cannot be deleted, but it can be deactivated in REACH-IT. To deactivate the pre-registration look for your substance in the pre-SIEF section of REACH-IT and use the ‘Deactivate’ functionality.

The Status column that describes the status of your participation in the pre-SIEF will turn to ‘Inactive’. You can reactivate you pre-registration at any time by using the ‘Activate ’ functionality. If you update your pre-registration while the status is inactive, the system will automatically reactivate your pre-registration.

The deactivation of a preregistration signals to other pre-SIEF members, that you are not interested in an active participation in the SIEF discussion. Note, however, that even as a non-active participant to the pre-SIEF you may still be asked to share data in the SIEF.

Note also, that the pre-registration and potential future registration of your substance are not affected by the deactivation from the pre-SIEF forum. You can benefit from the extended registration deadline if you have a valid preregistration, irrespective of its status (active or inactive).

The ‘Deactivate’ button is disabled if a third party representative was appointed for a particular pre-registration. In this case, the deactivation can only be performed by the third party representative and not by the potential registrant.

Can downstream users check online if their suppliers have pre-registered?

No, downstream users should make appropriate contractual arrangements with their suppliers to ensure that they comply with REACH.

Where can I see the list of substances that have been pre-registered?

Pursuant to Article 28(4) of the REACH Regulation, ECHA published a list of pre-registered substances on its website by 1 January 2009. The list includes all substances that were pre-registered by 1 December 2008. For each substance the following information is given:

  • Substance identification: EC number, CAS number and name of the substance
  • Substance identification of the similar substances, if applicable
  • First envisaged registration deadline

This list does not mention the names of the companies who pre-registered the substances. You are invited to check the list on our website at: http://echa.europa.eu/information-on-chemicals/pre-registered-substances

What should I do if I am in the wrong pre-SIEF?

If during pre-registration of your substance, you entered your substance name in a different way than the other manufacturers and importers, or if you realise during discussions on the sameness of your substance that you do not have the same substance as the other pre-registrants in the pre-SIEF, you may want to look for and join another SIEF. Whether you find a more suitable SIEF or not, you must register your substance with the correct identifiers, which have to be consistent with the analytical data on your substance.

A useful tool when looking for a more suitable SIEF is the list of pre-registered substances. This list contains all pre-registered substances, with the available identifiers, such as EC number, CAS number and chemical name with synonyms. The list is available at:

http://echa.europa.eu/information-on-chemicals/pre-registered-substances. You can also search the list of registered substance available at https://echa.europa.eu/information-on-chemicals/registered-substances.

Once you have examined the list of pre-registered and/or registered substances, the following scenarios are possible:

1) You found a more suitable pre-SIEF for your substance

You can find the lead registrant in the list of lead registrants on the ECHA website. Contact the lead to join the SIEF. If the substance is not listed or no lead is mentioned, you can use REACH-IT to update your pre-registration. If you add the more suitable substance as a similar substance you will have access to this substance pre-SIEF page. As you will not be listed as a member of this pre-SIEF, you will have to take the initiative and get in contact with the pre-registrants therein to explain that you wish to join the SIEF. It is also possible for you to set up the joint submission and to become the lead registrant. For instructions on how to update your pre-registration to view a different pre-SIEF in REACH-IT, see Q&A 1142.

2) You did not find a suitable pre-SIEF for your substance

Most likely you will have to become the lead registrant for the substance. In any case, you should include your pre-registration number in Section 1.3 of your IUCLID dossier, even though it previously corresponded to different substance identifiers (see Q&A 293)In addition, you should keep any relevant documentation that demonstrates the phase-in status of your substance in case it is requested by the enforcement authorities.

Vad gör jag om jag har hamnat i fel förhands-SIEF?

Om du har angett ämnesnamnet på annat sätt än övriga tillverkare och importörer vid förhandsregistreringen, eller om du under diskussionerna om huruvida det rör sig om ett likvärdigt ämne inser att ditt ämne inte är detsamma som övriga förhandsregistranters i ett förhands-SIEF, bör du leta reda på och registrera dig i ett annat SIEF.

Ett användbart verktyg när du söker efter ett lämpligare SIEF är förteckningen över förhandsregistrerade ämnen. Förteckningen innehåller alla förhandsregistrerade ämnen, med tillgängliga identitetsbeteckningar som EG-nummer, CAS‑nummer och kemiskt namn med synonymer. Förteckningen finns på webbadressen https://echa.europa.eu/information-on-chemicals/pre-registered-substances

När du väl har hittat en lämpligare eller mer specifik identitetsbeteckning för ämnet (som därefter betraktas som ett ”annat” ämne av Reach-IT) kan du använda Reach-IT för att visa förhands-SIEF för detta ”andra” ämne. För att kunna göra det måste du uppdatera förhandsregistreringen genom att lägga till detta ”andra” ämne i fliken för ”liknande ämnen”, som finns under ”Ändra förhandsregistrering”.

Från sidan för förhands-SIEF för ditt ämne kan du sedan gå till sidan för förhands-SIEF för detta ”andra” ämne. Du kommer inte att anges automatiskt som deltagare i detta förhands-SIEF, så du måste ta kontakt med förhandsregistranterna och förklara att du vill gå med i detta SIEF.

How can I become the SIEF Formation Facilitator (SFF) in REACH-IT and what are the tasks?

The SFF (SIEF Formation Facilitator) is the person initiating communication with other pre-SIEF participants to start working together and ultimately submit the data in a joint submission. The SFF is visible in the pre-SIEF page in REACH-IT and is marked with the letter F for Facilitator.

To take the role of SFF, use the ‘Become facilitator’ button from the Pre-SIEF page in REACH-IT. If the button is not available, it means that someone else is already the SFF.

If you are the SFF and you no longer wish to facilitate discussions among co-registrants, you should discuss with your co-registrants if anyone is willing to take up the role of facilitator. You can delete your role as facilitator by using the ‘Stop facilitator’ button.

For further info on the tasks of the SFF, see Q&A 99.

Can I still pre-register my substance?

According to Article 28(6) of the REACH Regulation, potential registrants who for the first time manufacture or import a phase-in substance in quantities of one tonne per year or more after 1 December 2008 can submit a late pre-registration within six months of first manufacturing or importing the substance above one tonne per year and at least 12 months before the relevant registration deadline.

The last registration deadline for tonnage bands between 1-100tpa is on 31.May 2018. This means that the deadline to late pre-register a new substance and benefit from the extended deadline expired on 31.May 2017.

If you are a potential registrants who for the first time manufacture or import a phase-in substance in quantities of one tonne per year or more you have submit your inquiry dossier to ECHA. For further information, see Q&A 444.

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