Staff members of CROMSOURCE are delighted to be contributing to the teaching of TOPRA’s Clinical Evaluation of Medical Devices Masterclass . By sharing our experience and knowledge we will help delegates understand how to achieve compliance with MEDDEV 2.7/1 revision 4 guidance on clinical evaluation, which was issued in June 2016 and is a key concern for manufacturers. Compliance with MEDDEV 2.7/1 revision 4 is a significant step towards compliance with the Medical Device Regulation’s more stringent clinical data requirements. More information about the Masterclass here: https://www.topra.org/TOPRA/TOPRA_Member/Events/Event_Display.aspx?EventKey=MC152017