ECVAM evaluation of GARDskin rescheduled to an extra scientific committee meeting in spring 2019
Lund, September 18, 2018 - SenzaGen (Nasdaq First North: SENZA) has been notified by the European Center for the Validation of Alternative Methods (ECVAM) authority that due to time constrains their scientific committee (ESAC) will not be able to evaluate tests in the category ”Test Guidelines on Health Effects”, to which GARDskin belongs, this year. The authority cites high workload as reason for the delay. Instead, ECVAM has announced that the evaluation of GARDskin is now scheduled for an extra meeting to be held during spring 2019.SenzaGen originally submitted the final validation