Every manufacturer, importer and Only Representative has REACH duties beyond the initial submission of a registration dossier. Maintaining your dossier is an essential part of compliance, particularly as new information emerges about your substance or its uses. ECHA also promotes the improvement of dossier quality and better compliance through its integrated regulatory strategy 2016.If your substance is on the Community Rolling Action Plan (CoRAP) for evaluation, has been selected for dossier evaluation through the common screening approach, or contained testing proposals, it is imperative that you understand how to manage the implications. Perhaps you have received a draft decision or a Quality Observation Letter (QObL) from ECHA, or new use information from your customers, or your substance is one of the hundred plus substances currently listed for review.This workshop will help you:
Discounted rates apply for REACHReady Gold subscribers and CIA members; book before 20 August 2018 for the early booking rate: £280 (+ vat) REACHReady/CIA members; £350 (+ vat) non members; thereafter £308/£385 (+ vat) respectively.