Andreas Emmendoerffer

Roche
Group Leader - Devices and Combination Products Regulatory
Andreas Emmendoerffer is a senior Regulatory Affairs professional with strong background in Medicinal Products, Medical Devices, Regenerative Medicine (Advanced Therapy Medicinal Products) and Quality Assurance, currently EU Group Lead DRA at Roche. He is a medical doctor with significant expertise in Immunology, Immunotoxicology, In vitro Toxicology and Inflammatory Diseases/ Oncology. Andreas has more than 20 years of international experience in regulatory affairs and quality assurance including pharma/ cell therapeutics and medical devices/ combination products. He also has more than 15 years of experience in Applied and Contract research, and more than 10 years hands-on experience and profound entrepreneurial background in business development of biotech/medtech start-ups, and direct leadership experience in international internal and external teams. Dr. Emmendoerffer possess recognized experience in medical device development, materials, biotechnological products (cytokines), cell therapeutics, cell- based systems and approval of clinical trials including first in man studies. He consistently demonstrates the ability to integrate strategic and global big picture thinking with operational and project management skills.