Advanced Therapies are promised to be one of the main pillars in the future of personalized medicine. Manufacturing and clinical evaluation of pharmaceutical products in this field, so called "Advanced Therapy Medicinal Products" (ATMPs), have to meet regulatory requirements of "Good Manufacturing Practices" (GMP) and "Good Clinical Practices" (GCP). The 3rd International Conference on "Strategies in Tissue Engineering" raises an excellent platform for discussion of these challenges. A specific session on "Clinical Studies and Regulatory Aspects" will focus exclusively on this topic and selected speakers will provide views and experiences from regulatory authority, clinical trial management and industry. Keynotes will
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