Accessibility
The extent to which information, services, technology, and environments can be perceived, understood, navigated, and used across human variation.
Professional glossary
Plain-language definitions used across this website. These are working professional definitions, not legal, regulatory, or clinical standards.
The extent to which information, services, technology, and environments can be perceived, understood, navigated, and used across human variation.
The degree to which information or an intervention can improve a meaningful clinical decision or outcome.
Explicit authority for making, approving, escalating, and reviewing defined organizational decisions.
A commitment to identifying and addressing avoidable, unfair differences in access, experience, quality, and outcomes.
The study of how genetic factors and their interaction with environments contribute to health and disease in populations.
The coordinated journey across eligibility, information, consent, collection, laboratory work, interpretation, results, counseling, referral, and follow-up.
The structures, responsibilities, standards, controls, and review processes through which decisions and risks are managed.
A coherent set of choices about outcomes, populations, services, capabilities, governance, resources, and performance.
The study and application of methods that support effective adoption, delivery, adaptation, and sustainability of evidence-informed practices.
A design approach that includes diverse needs and lived expertise from the beginning rather than adding accommodations at the end.
A perspective that considers how health opportunities and risks develop and interact across stages of life.
A structured explanation connecting resources and activities with outputs, intermediate changes, outcomes, and longer-term value.
The way capabilities, people, processes, decisions, technology, partners, governance, and measures work together to deliver strategy.
The health outcomes of a defined population and the distribution of those outcomes within it.
The use of individual and population information to improve prevention, diagnosis, treatment, or service decisions with appropriate evidence and governance.
Actions and systems intended to reduce avoidable risk, identify problems earlier, and support better health before crisis occurs.
The health, equity, experience, trust, capacity, and economic value created for populations and institutions.
A defined evidence threshold that must be met before an initiative advances, expands, changes, or stops.
A representation connecting a participant’s journey with the people, processes, technology, data, partners, controls, and decisions that enable it.
The complete sequence through which people discover, access, receive, and continue or exit a service.
A process in which people and professionals consider evidence, uncertainty, preferences, and circumstances together.
An explicit account of how and why an intervention is expected to produce intended outcomes in a given context.
A sequenced plan connecting strategic priorities with capabilities, initiatives, governance, measures, dependencies, and readiness.
Design that accounts for the complete service, its institutional context, dependencies, incentives, risks, and participant experience.