What is ECHA?
We are surrounded by chemicals and other substances daily. Unfortunately, some of those are hazardous. Our societies must control them and ensure proper safety. It is where ECHA comes to our rescue. Also known as the European Chemicals Agency, ECHA is a European Union regulation established in 2007. In short, ECHA works towards the safe use of chemicals. Indeed, ECHA legislations mean to protect human health and the environment.
How does ECHA Work?
Why ECHA?
First-of-all, let us discover why the European Union found a need to create ECHA. Per Title X, article 75 of the REACH regulation, ECHA:
[…] is established for the purposes of managing and in some cases carrying out the technical, scientific and administrative aspects of this Regulation and to ensure consistency at Community level in relation to these aspect.
The regulation in question here is REACH. Nowadays, ECHA also manages other requirements.
The ECHA Internal Organization
The ECHA Mission
The team of over 500 workers aims to improve chemical regulations. Here are examples of what ECHA does to protect both the people and the environment:
Legislations under the ECHA Management
ECHA has several enforced legislations and some convenient databases. Here are eight of them:
REACH, SVHCs, and Annex XVII
Adopted in 2007, REACH got enacted to improve the protection of human health and the environment from the hazards that chemicals can cause. In principle, REACH applies to all chemical compounds, not just those used in industrial processes. Indeed, it covers our daily life products, such as:
What is an Article?
The SCIP Database
As a result, the REACH regulation affects most businesses serving the EU market. As an importer, user, or seller, you may want to verify that the product you buy complies with REACH to avoid complications.
REACH targets so-called Substances of Very High Concern or SVHCs. SVHCs get added every six months to complete the list. If the SVHC declaration threshold in a product component is at or above 0.1% of weight by weight, it must appear on the public SCIP database.
REACH also contains another annex affecting articles, different from the SVHCs list. This annex provides a list of restrictions on the use of hazardous substances on the European market. It is known as REACH Annex XVII of the restricted substances list.
Understanding CLP
Lastly, the Classification, Labelling, and Packaging (CLP) regulations provide a high degree of health and environmental protection and the free movement of chemicals, mixes, and articles. The CLP’s primary goal is to assess whether material exhibits characteristics that lead to hazardous categorization.
Here is a step-by-step CLP classification:
Other Tools of ECHA
Over the years, ECHA has gathered much information on various chemicals for all their legislation. The ECHA support page may bring an answer to questions one might have on a specific substance and its restrictions. Moreover, ECHA has many other tools, like:
How to Create an ECHA Account
First-of-all, an ECHA account is necessary to access tools, receive notifications, or download certain documents.
There are four types of accounts:
- Authority accounts dedicated to governmental agencies, for example
- Industry accounts for companies
- Committee account for organizations like groups of experts or associations
- Personal accounts for individuals
To create an ECHA account for an industry:
- Click on the basic login page.
- Click on Create and ECHA account
- Enter your user details and create a password
- Then, you will receive an email verification link, and you will be able to log in
- You will access the ECHA central dashboard page, where you can give the credentials about your legal entity, like its:
- Name
- VAT number
- General contact information
- Address
- Security question
How to Prepare an Inquiry Dossier
- First, you must create an ECHA account (see above) with IUCLID.
- Then, you have access to IUCLID where you can prepare an inquiry dossier.
- Give your substance name to the new dossier and select REACH Inquiry from the TOC (table of contents) tab. Everything marked with a star (*) symbol s mandatory.
- Select or create a new reference substance with its formula, CAS number, and other chemistry details from the identification section.
- In the composition section, give details like the ingredients’ names, purity, and concentrations.
- Provide Analytical information by adding the type of analysis and method, like GC/MS.
- Then, give credentials about the substance production Site(s).
- Finally, detail your inquiry type (such as Inquiry for phase-in Substance that has not been pre-registered) in the Information Requirements tab.
Save your dossier! If no errors are detected, then you have completed your inquiry!
How to Act in Dossier Evaluation
Once a registrant submits a substance dossier, ECHA evaluates it following these fours steps :
- First, ECHA selects and assesses the prioritized substances dossiers and issues draft decisions of requested tests.
- Next, ECHA communicates to the registrants with deadlines to comply.
- Then, the registrants must have the tests performed within the deadlines.
- Finally, ECHA verifies the tests accordingly to its decisions.
In Conclusion
Overall the ECHA is here to improve EU chemical legislation and protect human health and our environment. By complying with their legislation or helping improve the existing tools, you can help too.
Do you have any questions about ECHA-related legislation or hazardous substances? Contact Enviropass!