Apply for product authorisation by the deadlines to keep your products on the NI market The following EU BPR active substance approval date is coming up: - N,N-Didecyl-N,N-dimethylammonium chloride (Didecyldimethylammonium chloride) (CAS 7173-51-5 EC 230-525-2) in product types 3 and 4
1 November 2022 If you supply biocidal products containing this active substance in the relevant product types, don't forget to apply for EU BPR product authorisation by the dates above to keep them on the NI market. Take action to keep your active substance in the EU Review Programme The active substance/product type combination listed below has been successfully notified into the EU Review Programme following an open invitation. The next step is for a full active substance dossier to be submitted to the European Chemicals Agency (ECHA) by the following deadline. This affects NI: - Brandy (CAS n/a EC n/a) in product type 19
5 May 2023 Only the person, company or taskforce/consortium that successfully notified the active substance/product type combination listed above can submit a dossier. If any of these active substance/product type combinations are important to you, consider contacting the notifier to let them know. You may even be able to join them in supporting the active substance. Check the ECHA list of notifications. If a dossier is not submitted by the deadline, this active substance/product type combination will be subject to an EU non-approval decision. Biocidal products containing active substances with EU non-approval decisions for the relevant product types will have to be removed from the NI market. HSE will provide separate updates on these where relevant. Make sure you are receiving important information about your product authorisations and approvals If you hold product authorisations and approvals in NI under the EU BPR or the Control of Pesticides Regulations (COPR), you should make sure HSE has the right contact details for you. If the details we hold are out of date, you may not receive important information about your product authorisation or approval. Update your details. | 
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