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Patient Data Autonomy

Meaning

Patient Data Autonomy is the ethical and legal right of an individual to exercise complete control and self-determination over their personal health information, including sensitive hormonal profiles, genetic data, and physiological monitoring metrics. This principle mandates that the patient must provide explicit, informed consent for the collection, storage, sharing, and use of their data by any clinical or technological entity. Empowering patients with this autonomy is crucial for building trust in the digital health ecosystem and ensuring that personalized hormonal wellness protocols are developed and maintained with the individual’s full partnership and consent. The patient is the ultimate steward of their own biological narrative.