The advancement of regenerative technologies demands careful alignment with societal values, legal frameworks, and business viability. Ethical, regulatory, and commercial aspects address questions of patient consent, long-term safety, equitable access, and sustainability of emerging therapies. The global expansion of clinical trials and biotechnological innovation calls for harmonized approval processes and transparent standards. Commercial strategies must balance profitability with public good, encouraging innovation while maintaining accountability. Ethical, regulatory, and commercial aspects also include intellectual property rights, pricing models, and education for both clinicians and patients. Navigating this complex terrain is essential for responsible translation of regenerative science into accessible and ethically sound healthcare solutions.
Title : AI-integrated high-throughput tissue-chip for space-based biomanufacturing applications
Kunal Mitra, Florida Tech, United States
Title : Stem cell technologies to integrate biodesign related tissue engineering within the frame of cell based regenerative medicine: towards the preventive therapeutic and rehabilitative resources and benefits
Sergey Suchkov, N.D. Zelinskii Institute for Organic Chemistry of the Russian Academy of Sciences, Russian Federation
Title : In vitro evaluation of lyophilized Dedifferentiated Fat cells (DFAT) impregnated artificial dermis
Kazutaka Soejima, Nihon University, School of Medicine, Japan
Title :
Nagy Habib, Imperial College London, United Kingdom
Title :
Alexander Seifalian, Nanotechnology & Regenerative Medicine Commercialisation Centre, United Kingdom
Title : The regenerative medicine of the future
Marco Polettini, DVM, Italy