REACH
Overview
Registration, Evaluation, Authorisation and Restriction of Chemical substances (REACH) is a European Community Regulation (EC 1907/2006) that became effective on June 1, 2007. It replaces a number of fragmented European directives and regulations within a single system. The main objective of REACH is to improve the protection of human health and the environment through:
- collection and sharing of chemical substance data throughout supply chains, and
- authorization or restriction of chemicals of higher concern.
What distinguishes REACH from previous rules are:
Here is how the system will be administered:
The ultimate driver for REACH is the authorization or restriction of substances. Substances of very high concern (SVHC) cannot be used or placed on the EU market without a specific authorization, granted from ECHA. In some circumstances restrictions will apply and some substances, based on their risks to humans and the environment, will be banned.
Impacts on U.S. Manufacturers/Exporters
REACH is expected to have world-wide impacts. When it is fully in force, REACH will require all companies manufacturing/importing chemical substances into the European Union in quantities of one metric tonne (2,205 lbs.) or more per year (or substances already classified as dangerous over 100 tonnes per year) to register these substances with the European Chemicals Agency. Because REACH applies to some substances that are contained in articles (e.g., autos, batteries, telephones), any company importing goods into Europe could be affected.
Potential registrants (i.e. manufacturers and importers of chemical substances) must “pre-register” these substances by December 1, 2008, in order to benefit from postponed “phase in” deadlines. These deadlines depend on the classification and quantity of the substance supplied – the deadlines are set out in the timeline below as phases 1, 2 and 3.
Although pre-registering is not mandatory, it is free, and it is an important step in allowing potential registrants much more time before they have to fully register.
The registration process is based on the principle of “one substance, one registration” (OSOR). Consequently, all firms which pre-register the same substance will be encouraged to work together to register the substance which includes the sharing of data.
There are many exemptions from many or all of the provisions of REACH. Some substances being structurally simple and benign are exempted (and listed in the Annexes to the Regulation). Other chemicals or preparations already regulated are exempt from certain provisions such as those in medicinal products or in foods.
Table 1. REACH Timeline
Date |
Action |
June, 1, 2007 |
REACH became effective |
|
November 30, 2008 |
Pre-registration for ‘phase-in’ substances ends |
December 1, 2008 |
Registration for existing substances (that have not been pre-registered) starts |
January 1, 2009 |
List of pre-registered substances published and SIEFs are formed |
June 1, 2009 |
First recommendation of priority substances to be considered for authorization published by ECHA |
Phase 1 |
By this date the following pre-registered ‘phase-in’ substances should have been registered when supplied at:
|
Phase 2 |
Deadline for registration of substances supplied at ≥ 100 tpa |
Phase 3 |
Deadline for registration of substances supplied at ≥ 1 tpa |
More Information
What REACH means for Manufacturers What REACH means to EU importers The European Commission supports businesses affected by REACH by providing free of charge a software application (IUCLID), which simplifies capturing, managing and submitting of data on chemical properties and effects. Automotive Industry Action Group. In response to the REACH regulation, AIAG has formed an industry consortium to help U.S. manufacturers understand the new requirements.