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REACH stands for Registration, Evaluation, Authorisation and Restriction of Chemicals adopted in December 2006. REACH Regulation (EC) No 1907/2006 and Directive 2006/121/EC amending Directive 67/548/EEC were published in the official Journal on 30 December 2006. Enterprises which manufacture or import more than one tonne of a chemical substance per year will be required to register it in a central database administered by the new EU Chemicals Agency. Registration: Around 30000 estimated substances produced or imported into the EU at 1 tonne /year has to be registered. Registration deadlines for substances produced or imported to EU:- First year of entry into force (1 June 2007) to year 3: Substances of greater hazard which are produced or imported to EU at the rate 1000 tonnes and CMR (carcinogenic, mutagenic or toxic to reproduction ) 1 tonnes have to be registered along with relevant testing documents. From year 3 to year 6: Substances produced or imported to EU at rate of 100 tonnes – 1000 tonnes have to be registered . From year 6 to year 11: Substances produced or imported to EU at rate of 100 tonnes will be registered. A non phase-in substance is a completely new substance that has neither been used nor registered in the market before the entry of force of REACH. What is REACH? * Evaluation: Will require the submission of additional data – could be substantial. Prioritization criteria to take account of Tonnage. Hazard and exposure. Potential risk to human health or the environment. Dossiers for substances with volumes 100 tonnes will be subjected to an evaluation by the relevant national authorities. Where an authorities believes that the risk of using a substances is expected to be high e.g. due to the structure of the substance, they can carry out a more detailed assessment. Authorization: Substances of high concern must be authorized for use at an EU or national level, e.g. CMR’s(carcinogenic, mutagenic or toxic to reproduction), PBT’s(p