ufi code regulation

following ingestion), appointed bodies should have at their disposal information on the latter components where needed to formulate preventive or curative action.

The Commission carried out the review provided for by Article 45(4) of Regulation (EC) No 1272/2008, and its findings, which were based on thorough expert consultation, were published in January 2012. The submission format shall address the following elements: 1.2. In view of the fact that mixtures classified as hazardous may also contain non-classified components that can nonetheless have adverse effects after unintended use (e.g. By derogation from the second subparagraph, in a group submission, perfume or fragrance components in mixtures shall be present in at least one of the mixtures. It shall be submitted by electronic means in an XML format provided by the Agency and made available free of charge. The Agency shall provide technical and scientific guidance, technical support and tools facilitating the submission of information. How to create the UFI code. Hibiscus Plc is ready to support you with the production of labels, and authoring of Safety Data Sheets, to allow a smooth transition into compliance for 2020 onwards. Biocidal Products Committee opinions on active substance approval, National authorisation and mutual recognition, Understanding the Waste Framework Directive, List of substances subject to the POPs Regulation, Draft recommendation for inclusion in the Authorisation List and consultation, Submitted restrictions under consideration, Harmonised classification and labelling targeted consultations, Consultations on ECHA Executive Director’s requests, PACT - Public Activities Coordination Tool, Information on Candidate List substances in articles, Candidate List of substances of very high concern for Authorisation, Registry of restriction intentions until outcome, Registry of SVHC intentions until outcome, Table of harmonised entries in Annex VI to CLP, Occupational exposure limits - Activity list, Harmonised classification and labelling (RAC), Applications for authorisation consultations, Harmonised classification and labelling consultations, ECHA Executive Director’s requests related to the CLH process, Consultation on potential candidates for substitution, Consultation on derogation to the exclusion criteria, ECHA's Executive Director Requests to the Committees, Consultation on a draft recommendation for amendment of Authorisation List entries, Consultations in the authorisation process, Occupational exposure limits - Call for comments and evidence, Occupational exposure limits - Previous calls for comments and evidence, Occupational exposure limits – Consultations on OEL recommendation, Derogations for the protection of cultural heritage, ECHA's current activities on restrictions, ECHA's completed activities on restriction, Information on Candidate List substances in articles table, Information from the Existing Substances Regulation (ESR), PBT/vPvB assessments under the previous EU chemicals legislation, Adopted opinions and previous consultations on applications for authorisation, Adopted opinions on restriction proposals, Mapping exercise – Plastic additives initiative, Occupational exposure limits substance evaluations, List of substances subject to POPs Regulation, Small and Medium-sized Enterprises (SMEs), Practical examples of chemical safety reports.

2.2. 3.2.

The marking has to be clearly visible and legible on the label. if a change in the composition of the mixture fulfils one of the following conditions: addition, substitution, or deletion of one or more components in the mixture that shall be indicated in accordance with Section 3.3; change in the concentration of a component in the mixture beyond the concentration range provided in the original submission; the exact concentration of a component was provided in accordance with Sections 3.4.1 or 3.4.2, and a change occurs to that concentration beyond the limits identified in Table 3. The submission shall include the information on the toxicological effects of the mixture or its components that is required in Section 11 of the Safety Data Sheet of the mixture, in accordance with Annex II to Regulation (EC) No 1907/2006.

5.1. The submitter shall create a unique formula identifier, hereinafter UFI, by electronic means made available by the Agency. What is the Classification and Labelling Inventory?

Regulation (EC) No 1272/2008 is amended as follows: In Article 25, the following paragraph 7 is added: ‘7. The classification of mixture components for health and physical hazards (hazard classes, hazard categories and hazard statements) shall be provided.

In the case of a limited submission as laid down in Section 2.3 of Part A, a telephone number and an email address for rapid access to additional detailed product information services shall be provided at which rapid access to detailed additional product information in the language provided in Section 3.3 of part A is available for appointed bodies during emergencies.

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