Stem Cell & Regenerative Medicine

Ethical, Regulatory & Quality Control Frameworks

Ethical and regulatory considerations are critical for the safe translation of regenerative therapies. This session focuses on guidelines governing stem cell research, gene editing, tissue engineering, and clinical trials. Key topics include informed consent, patient safety, standardization of manufacturing, and compliance with international regulatory bodies. Quality control ensures reproducibility, efficacy, and safety of cellular and tissue-based therapies. Emerging challenges involve balancing innovation with ethical responsibility, addressing long-term follow-up, and ensuring equitable access. Attendees gain insights into frameworks that guide ethical research, clinical translation, and commercialization of regenerative medicine products.