Since October 1st, 2014, we have been included in the OsSC register of private laboratories qualified for the analysis of samples from clinical trials on drugs (phases I-II-III) by the AIFA, conforming to articles 1 and 2 of the DM 16 Marzo 1998.

GEM FORLAB is part of the European regulatory platform for clinical trials called CTIS. The Clinical Trials Information System (CTIS) is a computer system developed by the European Medicines Agency (EMA) for managing and supervising clinical trials within the European Union (EU) and the European Economic Area (EEA). CTIS is designed to facilitate the application of the Clinical Trials Regulation [Regulation (EU) No 536/2014], which aims to create a more coherent and harmonised environment for conducting clinical trials.