Unlike new medical devices and pharmaceutical interventions, not all healthcare technologies undergo a rigorous clinical approval process. As a result, certain technological interventions may not be grounded in scientific evidence, potentially leading to harmful effects and costly interventions without benefit for those who use them.
The future of health technologies requires accountability mechanisms to ensure quantifiable health impacts. National and international stakeholders must come together to create regulatory frameworks and set ethical industry norms. The path forward must include review and evidence standards that are equivalent to the stringent scientific standards for medical devices. These methods can help assuage the hesitancy and scepticism many in the public feel about healthcare technologies by helping to prove their benefits.