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Lead RegistrantThe lead registrant takes on the legal responsibility under Article 11 of REACH for executing joint submission in time so that other registrants can follow suit in due course. The Cefic recommended deadline for the joint submission of high volume, CMR 1 and 2 and R 50 and 53 substances is 1st June 2010. Yet, currently less than 10% of pre-registered substances have a Lead Registrant. Some lead registrants can rely on the support of a consortium, industry association or a research institute. Others have been alone in initiating pre-SIEF activities. Depending on our customer’s need, we provide support for lead registrants through the critical path to registration and beyond. As a first step for companies considering the option of taking the role of lead registrant we recommend our lead registrant risk analysis. If you have any questions, please contact us. |
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