Full Name
                                                    Mr. Maurizio Andreano
                                                    Job Title
                                                    Sen. Director Technical Regulations & Standardization
                                                    Company
                                                    Siemens Healthineers AG
                                                    Speaker Bio
                                                    Maurizio is a Senior Director at Siemens Healthineers and their global Head of Technical Regulations & Standardization. 
Born in Germany and educated in law and international business in various countries, he joined the MedTech industry twenty years ago, setting up the EU Chamber of Commerce in China Healthcare Group and subsequently the COCIR China Desk in Beijing. After several years in China and two years in Brussels at COCIR, he joined in 2010 Siemens Healthcare as Director of External Affairs in Germany. Passionate about standards and regulations he is a member of the IMDRF Standards Working Group and the German Commission for Electrotechnical, Electronic & Information Technologies.
Maurizio believes in active dialogue for the benefit of patients who depend on medical devices worldwide. He is a Member of the DITTA Board of Directors and the Co-Chair of the DITTA Standardisation Working Group. In the past he also served as member of the EU New & Emerging Technologies Group (MDCG) as well as the CEN/ CENELEC Advisory Board for Healthcare Standards.
                                                    Born in Germany and educated in law and international business in various countries, he joined the MedTech industry twenty years ago, setting up the EU Chamber of Commerce in China Healthcare Group and subsequently the COCIR China Desk in Beijing. After several years in China and two years in Brussels at COCIR, he joined in 2010 Siemens Healthcare as Director of External Affairs in Germany. Passionate about standards and regulations he is a member of the IMDRF Standards Working Group and the German Commission for Electrotechnical, Electronic & Information Technologies.
Maurizio believes in active dialogue for the benefit of patients who depend on medical devices worldwide. He is a Member of the DITTA Board of Directors and the Co-Chair of the DITTA Standardisation Working Group. In the past he also served as member of the EU New & Emerging Technologies Group (MDCG) as well as the CEN/ CENELEC Advisory Board for Healthcare Standards.
Speaking At
                                                    
                        