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Global innovations and challenges in regenerative medicine

Highlighting global innovations and challenges of regenerative medicine to create a harmonized regulatory framework

There is a need to develop clear and robust regulations to guide the translation of regenerative medicine (RM) research into interventions that improve public health. While regulatory frameworks exist for clinical trials and marketing of RM products, attention is needed to address the specific challenges posed by these emerging technologies. Our work examines RM policy and governance across regions of the Global South to understand the regulatory approaches, innovations and challenges that RM brings. By focusing on under-examined areas in literature, this study aims to contribute to global discussions on RM government and support the development of inclusive and well-suited regulatory frameworks. 

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