CLP has spawned a host of useful, and a few not so useful, sources of information. Some are essential for reference, some for learning, and some for leaving until (much) later. We think you need to make the most of your time, so here are some comments and a summary to help you find your way through the CLP Guidance and information maze.
Again our ’A brief guide to CLP’ will help. Then we suggest you read the ECHA Questions and Answers on CLP. It will enable you to identify your role in CLP and begin to map out the work you need to do.
If your interest is anything to do with business we now suggest our advice on developing a business plan (see CLP Briefing Note: Making a business plan). We then suggest you now refer to our topic-based webpages and Briefing Notes depending on the subject of interest:
Alternatively if you still want an overview you may want to read the ECHA Introductory Guidance on the CLP Regulation. This is a substantial document and you need to set aside a couple of hours to read and digest it. You may want (but you don’t need) to access the Regulatory text as well to cross refer as you go along. When you have read this document you should be able to scope your CLP tasks and (with the rest of our guidance) identify the resources required.
For an overview of classification read our Guidance on Classification. After that you need to use both Annex I of the Regulation and the ECHA Guidance on the Application of the CLP Criteria. But take care! The latter is a long (winded) document with a good deal of expert scientific discussion, some of it highly specialised. It certainly can’t be read at one sitting! The introduction is valuable for its general advice but we regard the rest of the Guide as a resource manual for the expert or for use to progressively learn and expand your knowledge, perhaps supported by some formal training. You will cross refer to Annex I of CLP as you use the Guidance and you should find this Annex a relatively easy read once you have grasped the terms and basic layout.
For an overview go to our Guidance on Labelling. After that the ECHA Guidancee to Labelling and Packaging is the document you need. You will need the classification of the product (which you could obtain from an expert colleague) and know its use. You will also need a copy of the Regulation including the Annexes. With this information you should be able to draft out labels and prepare for practical artwork.
We have prepared both a Guidance document and a practical Online Step-by-step guide on notification. If you want more then read the helpful ECHA Practical Guide 7: How to Notify Substances in the Inventory. This document is straightforward and well written and you should be able to work though it in a couple of hours. You may want to be able to access REACH-IT as you go through the documents.
Then please go to either our FAQs or the ECHA Frequently Asked Questions prepared by ECHA.
Then ask them by using the list of National Helpdesks from ECHA. But don’t expect a prompt reply – some of the helpdesks take weeks to respond and in some cases it’s difficult even to ask a question. Most CAs also have websites and some (e.g. France and UK) have helpful newsletters to which you can subscribe.
How about our CLP Briefing Note to set the scene!
After that it’s tempting to find a copy of the Regulation and to plunge in. Our advice is: STOP! Only do this if you are competent at classification under the previous system, you understand the background to CLP, and are comfortable working with legal texts. If all this is the case then visit our Legislation webpage for the full 2008 text of CLP. There you will also find the current subsequent Adaptations to CLP which altered some of the Annexes to the Regulation. Unfortunately, there is no single legal document which consolidates these texts. However a database of the updated entries in Annex VI can be accessed via the ECHA Classification and Labelling Inventory – but note this is not a formal legal text. You will need to use the tab ” GHS/CLP” and follow the dropdown menu “search Annex VI”.
We hope that this guidance will help our subscribers to notify their substances directly in REACH-IT. If you don’t need to claim confidentiality on the IUPAC name of your substance, the REACH-IT
Classification is all about evaluating and identifying the hazards of a chemical. But users need basic information about the chemical and its supplier and practical handling advice on the packaging. To provide a consistent approach, CLP sets down basic rules on how this information must be communicated; and examples of ...
Classification and labelling of substances has been part of EU law for more years than most of us have worked, and it has gone through many step changes. We are used to the hazard warning labels found on household bleach and some other household chemicals, but we know we don’t ...
From 1 December 2010, the Classification, Labelling and Packaging (CLP) Regulation progressively replaced the Dangerous Substances and Dangerous Preparations Directives (DSD, DPD) which were repealed from 1 June 2015.
It’s tempting to find a copy of the Regulation and to plunge in. Our advice is STOP! Only do this if you are competent at classification under the previous system (DSD/DPD), you understand the background to CLP, and are comfortable working with legal texts. If so, then the full text ...
Notification is a new requirement that was introduced by CLP (Articles 39 and 40). The basic obligation applies to EU/EEA legal entities who manufacture and supply, or import, substances (including in some mixtures) after 1 December 2010. They have to notify core information which identifies the substance and its hazard ...
If you have global responsibility for classification and labelling, then you MUST know something about the source of CLP: the UN GHS system for classification and labelling. We suggest you visit the UN website and briefly read the introductory notes.
You can call our Helpdesk number on +44 (0) 20 7901 1444. Or e-mail us on enquiries@reachready.co.uk.