Turkey KKDIK regulation shares the same principle as EU REACH: One substance, One Registration to reduce the amount of animal testing. Therefore, under KKDIK, members of a Substance Information Exchange Forum (SIEF) will have to appoint a Lead Registrant. Like in EU REACH, under KKDIK, the lead registrant will be responsible for preparing the lead dossier of the joint submission and for gathering all physicochemical, toxicological and eco-toxicological data on the substance(s) and its uses. In some cases, companies may organise themselves into a consortium to develop the lead dossier and collect the required data etc.
Join our online event! We invite all companies willing to take the Lead registrant role for KKDIK registration purposes to join our event. During our online session, we will explain the steps companies need to take to nominate themselves as Lead Registrants and information required to be included in the Lead Dossier.
Topics to be addressed: • KKDIK Regulation – Focus on Lead Registrant Obligations • KKDIK Lead Registration – How will this work in practice • Compliance Strategies for companies willing to take the lead role • Conclusions • Q&A
Speaker: Frederik Johanson, REACHLaw *Please note that this webinar is not meant for REACH consulting companies or service providers