REGARTIS / EcoMole Ltd.
About this exhibitor
REGARTIS / EcoMole Ltd. is a consulting company, providing services in the field of chemical regulations.
Our main areas of business are REACH, UK REACH, CLP, Biocides and other legislations.
We are providing services all around the world since REACH came into force in 2006. In the United Kingdom, we operate through our branch company EcoMole Ltd. REGARTIS together with EcoMole are your reliable guide through the minefield of chemical regulations on both sides of the Channel.
Product & Services
UK REACH
Do you import products to the UK or buy raw materials here? And did you know that as a result of Brexit you have to meet the requirements of the new chemical law, UK REACH? We will provide you with a complete portfolio of services related to the transition to the new British REACH. Whether it is the services of an exclusive representative, auditing, registration or authorization.DUIN Downstream User Import Notification is intended for importers, downstream users and distributers seated in Great Britain or with an Only Representative there, that have already been importing the substance to Great Britain before the transition period before Brexit. By submission of this notification, these companies can postpone their registration obligation for these substances by 2, 4 or 6 years from 28.10.2021. HSE doesn’t charge any fees for this notification. We can take care of the whole notification for you. We need only the available information about the substance like the identification numbers, imported tonnage when it’s possible also SDS or analytical reports. If you’re not seated in Great Britain, we can also provide the Only Representative service. The time needed to complete DUIN depends on the number of substances, but we generally complete it within few days. We’ve been doing this since the beginning of 2021, so from the very beginning and you can also watch our recorded webinar series about UK REACH. It’s important to say, that the deadline for DUIN submission in on 28 October 2021. Don’t hesitate to contact us and we will take care of it!
Find out moreProduct stewardship
Hand over your chemicals portfolio regulatory compliance to us. Your products will be taken care of with utmost care, one could even say that we will spoil them a little. We will follow the changes in relevant regulatory affairs and suggest or perform necessary changes to assure your compliance. Moreover, we will provide you with regular updates and news.Continuous care Hand over your chemicals portfolio regulatory compliance to us. Your products will be taken care of with utmost care, one could even say that we will spoil them a little. We will follow the changes in relevant regulatory affairs and suggest or perform necessary changes to assure your compliance. Moreover, we will provide you with regular updates and news.Chemical audit First, let's build a map and a list: a comprehensive overview of chemicals in your company. Then we will define requirements according to REACH, CLP, and Czech national legislation. We will check how you comply with such requirements and report them in the dossier with proposals to raise compliance. All this with respect to current processes implemented in your company.
Find out moreEU REACH
We provide complex services to ensure your compliance with the REACH Regulation (EC 1907/2006). From Registration to Authorization.
Find out moreCLP
CLP (short for EU Regulation 1272/2008 on Classification, Labeling and Packaging of substances and mixtures) is a system for assessing the hazards of a substance and mixture. This assessment is needed for safe handling, storage and creation of safety data sheets. The classification is also related to the labels of substances and mixtures.CLP (short for EU Regulation 1272/2008 on Classification, Labeling and Packaging of substances and mixtures) is a system for assessing the hazards of a substance and mixture. This assessment is needed for safe handling, storage and creation of safety data sheets. The classification is also related to the labels of substances and mixtures.We have been performing the classification for a really long time, in the CLP system from the very beginning, we apply all amendments, including UFI codes and related obligations.In addition to our own hazard assessment of substances and mixtures, we also perform classification checks in our customers' sheets, prepare and check labels, all in different languages.There are really many substances and mixtures for which we have performed this hazard assessment, for some customers, we also provide a permanent service.The issue of CLP is not simple, but we are happy to help you with it at any time.
Find out morePoison Centres Notification
The EU has harmonized the information requirements on mixtures classified as hazardous for human health or physical effects as of 2021. Article 45 and Annex VIII to the CLP Regulation identify EU importers and downstream users of certain hazardous mixtures on the market as responsible for the submission of the information to appointed bodies.The required information includes the clear identification of the mixture, information on the full composition and hazardous ingredient substances, and the intended use through a system of harmonized categories. The information must be submitted by electronic means in a specified format, which enables the appointed bodies to easily retrieve the relevant information. A unique formula identifier (“UFI”) which is linked to a valid submission, and placed on the label or the packaging, will allow the poison centers to unambiguously identify the composition of the mixture and propose the appropriate medical treatment in the event of poisoning.The date of applicability depends on the use type of the mixture: 1 January 2021 for consumer or professional use 1 January 2024 for industrial use If you are placing hazardous mixtures on the market, you will have to prepare information in an EU-harmonised Poison Centres Notification (PCN) format.How can REGARTIS help? We canProvide you with a complex service of PCN notification, by compiling the SDS in accordance with requirements of effective legislation in different MS languages (optional) generating the UFI code preparing the PCN dossier submitting the information through ECHA’s submission portal Advice you on the PCN preparation Organize an in-house/online training and teach you how to prepare PCN notification
Find out moreSCIP Notification
SCIP is the database for information on Substances of Concern In articles as such or in complex objects (Products) established under the Waste Framework Directive (WFD). Companies supplying articles containing substances of very high concern (SVHCs) on the Candidate List in a concentration above 0.1% weight by weight (w/w) on the EU market must submit information on these articles to ECHA, as from 5 January 2021.The SCIP database ensures that the information on articles containing Candidate List substances is available throughout the whole lifecycle of products and materials, including at the waste stage. The information in the database is then made available to waste operators and consumers. ECHA has established a harmonized IUCLID format for submitting the required information to the SCIP database.Suppliers of articles need to submit the following information to ECHA:information that allows the identification of the article the name, concentration range, and location of the Candidate List substance(s) present in that article other information to allow the safe use of the article, notably information to ensure proper management of the article once it becomes waste
Find out moreSDS management
We are able to compile any number of Safety Data Sheets for you in all of the languages of the EU. We can also build the Exposure Scenario for your substance or information on safe use for your mixture.Or we take over all of your SDS, update them on regular basis and whenever needed in order to keep them compliant with the latest regulations. You will no longer need to take care of SDSs. Ask for detailed information.
Find out moreBPR
Understanding biocidal legislation is quite challenging. If you want to market biocidal products in the EU or the UK and need advice or help, you are in the right place.Understanding biocidal legislation is quite challenging. If you want to market biocidal products in the EU or the UK and need advice or help, you are in the right place.Placing biocidal products on the EU market is regulated by regulation No. 528/2012 (in short BPR). A biocidal product is a substance or a mixture with the intention of destroying, deterring, rendering harmless, preventing the action of, or otherwise exerting a controlling effect on, any harmful organism by any means other than mere physical or mechanical action. The biocidal product contains a biocidal active substance or substances causing this effect.Biocidal products placed on the EU market can contain only active substances listed on the List of Active substances (Annex II Regulation No. 1062/2014). All active substances must be approved for their use (Product Type – PT) or evaluated. If the substance is not on the list or there is no intended use, a new application must be submitted. The process is named Approval of Active Substance. When the active substance is approved, the biocidal product must be authorized before placing on the EU market. The process is called Biocidal Product Authorization.BPs containing ASs in review program can be placed on the EU Member states markets following national rules. This process is called Biocidal Product Notification.Suppliers of ASs have to be listed in the List of AS and Suppliers, regardless, whether the biocidal product is notified or authorized.
Find out moreISO 50001
ISO 50001 Energy management systems – Requirements with guidance for use is a specification created by the International Organization for Standardization (ISO) for an energy management system.ISO 50001 Energy management systems – Requirements with guidance for use is a specification created by the International Organization for Standardization (ISO) for an energy management system. The standard specifies the requirements for establishing, implementing, maintaining and improving an energy management system, whose purpose is to enable an organization to follow a systematic approach in achieving continual improvement of energy performance, including energy efficiency, energy security, energy use and consumption. The standard aims to help organizations continually reduce their energy use, and therefore their energy costs and their greenhouse gas emissions.ISO 50001 was originally released by ISO in June 2011 and is suitable for any organization, whatever its size, sector or geographical location.[2] The second edition, ISO 50001:2018 was released in August of 2018.
Find out moreEndocrine Disruption Basics:
Helping you assess products for endocrine disruption properties.
Find out moreDon't let SVHC concern you!
Besides providing hands-on trainings and/or notifying the SVHCs to ECHA on your behalf, our experts are happy to help you with complete SVHC data management – assessing how to incorporate the SVHC notifications to ECHA into your existing business processes and data workflows. Including the system-to-system notification, where our team of chemical informaticians can link your existing systems to the ECHA SCIP database to allow automatic or semi-automatic notifications for sustained compliance whenever your product documentation is updated. Long story short, if you need any kind of help with SCIP, any time of year, just drop us a message!
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