These substances can therefore be used for any IRIS submission, for example to request a new Research Product Identifier (RPI). If you do not find the substance you need, please register it by completing the “ Substance Request Form ” and raising a request via the EMA Service Desk portal, for the substance to be included in the SMS database, attaching the Substance Request Form.

To be legally manufactured or imported in the EU, all substances within the scope of REACH have to be registered. Depending on the volume placed on the market, manufactures and/or importers, as part of their registration, must submit information on both human health and environmental effects, and hazardous nanoforms – an estimation of exposure throughout the life cycle.

The Medical Devices and the In-Vitro Diagnostic Devices Regulations have introduced new responsibilities for the European Medicines Agency (EMA) and national competent authorities in the assessment of certain categories of medical device. For an easier handling, the list of Pre-registered substances is available in four parts ordered by EC number. They contain the same information as the following full list. PRS List in CSV, part 1/4 (3.5MB), EC Numbers from 200-001-8 to 249-999-7 In urgent cases, please submit your question through the contact form. You can also call the ECHA Switchboard: +358 9 6861 80. Please follow our Twitter account @EU_ECHA for updates. Substances listed in EINECS/ELINCS/NLP are deemed as phase-in or existing substances in Europe and they can enjoy extened registration deadlines until 2018 if they were pre-registered under the EU REACH regulation.

Since 1 January 2020, before manufacturing or importing a nanoform of a substance, the operators concerned must submit the required nano-specific information to ECHA in a new or updated registration dossier. Last updated 30 March 2021. Database contains 25831 unique substances and contains information from 97818 dossiers.

Before an active substance can be used within a plant protection product in the EU, it must be approved by the European Commission. For an easier handling, the list of Pre-registered substances is available in four parts ordered by EC number.

av MRLKA Palm · Citerat av 21 — Source: Product Register, Swedish Chemicals Inspectorate, Sweden EU. As evident from Figure 7, import in such products may still be possible from other.

75 40210 Duesseldorf Germany : Germany : Active (1,2-Dioxoethylene)bis(iminoethylene) bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) 274-572-7 : 70331-94-1 : 2018 : View substance registered dossier: SI Group DEAB (Imp) Teplitzer Strasse 84478 Waldkraiburg Germany : Germany : Active 2020-08-14 · As a manufacturer or importer registering such substances, you must show the European Chemicals Agency (ECHA) how they can be used safely and use a safety data sheet to inform potential users in the supply chain of any risk management measures they may need to take. If your business is a downstream user, you have different obligations to meet. All approved active substances are listed in Implementing Regulation (EU) No 540/2011 and included in the EU Pesticides Database. A Review or Renewal Report is also prepared for each active substance during the decision-making process, providing details of the evaluation process and outcome.

Substances listed in EINECS/ELINCS/NLP are deemed as phase-in or existing substances in Europe and they can enjoy extened registration deadlines until 2018 if they were pre-registered under the EU REACH regulation. The REACH Registered Substances List and Pre-registered Substances List can be found on ECHA's website. Companies can check whether their substances have been pre-registered or registered by other companies.
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Registered substances information As substances are registered under REACH, there is an obligation on registrants to provide information on the substances they manufacture or import. ECHA subsequently has the obligation to make certain of this information publicly available. View substance registered dossier [Confidential] - - - (1S)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene : 207-856-6 : 498-15-7 - View substance registered dossier: Commentz & Co. GmbH & Co. Billbrookdeich 122 22113 Hamburg Germany : Germany : Active (1S)-3,7,7-trimethylbicyclo[4.1.0]hept-3-ene : 207-856-6 : 498-15-7 - View substance registered dossier View substance registered dossier [Confidential] - - - (17β)-3-{[alkyl(dimethyl)silyl]substituted}estratetraen-17-ol - - - View substance registered dossier: RSI ChemRep Europe Ltd (S001) 27-30 Merchants Quay Merchants House 8 Dublin Ireland : Ireland : Active (aminoalkyl) hydrogen thiosulfate - - 2017; 2021 : View substance registered dossier For an easier handling, the list of Pre-registered substances is available in four parts ordered by EC number.

By clicking the following link, you can search: List of Pre-registered Substances; Information on Registered Substances; The EU Pesticides Database allows users to search for information on active substances used in plant protection products, Maximum Residue Levels (MRLs) in food products, and emergency authorisations of plant protection products in Member States. Users can use the following search options to find information: Active substances View substance registered dossier: Croda EU B.V. (OR8) Buurtje 1 2802 BE Gouda Netherlands : View substance registered dossier: Rianlon GmbH : Charlottenstr. 75 40210 Duesseldorf Germany : Germany : Active (1,2-Dioxoethylene)bis(iminoethylene) bis(3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate) 274-572-7 : 70331-94-1 : 2018 : View substance registered dossier: SI Group DEAB (Imp) Teplitzer Strasse 84478 Waldkraiburg Germany : Germany : Active This database contains classification and labelling information on notified and registered substances received from manufacturers and importers.
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For the substances referred to in the first paragraph, the notified body shall, having verified the usefulness of the substance as part of the medical device and taking account of the intended purpose of the device, seek a scientific opinion from one of the competent authorities designated by the Member States or the European Medicines Agency (EMEA) acting particularly through its committee in

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