We are generating more data about people’s health and biology than ever before. Combined with advances in IT and data science, this offers significant opportunities to generate new knowledge and improve medical practice; but it also raises concerns about individuals’ privacy.
This report looks at the ethical issues raised by data use in biomedical research and health care. It sets out key ethical principles for the design and governance of data initiatives, and identifies examples of good practice relevant to anyone approaching a data initiative.
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