date:Apr 16, 2014
availability, toxicity and exposure. Under European law when such a request is made, the clock on the regulatory timetable for risk assessment is stopped until the applicant supplies the necessary information. The new procedure comes into force on 1 May 2014.
This initiative is important because a growing part of EFSAs work involves the evaluation of regulated products, so-called because they require scientific risk assessment by the Authority before they can be authorised by risk managers for