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Delivering responsible data through the National Data Strategy
Examining how the commitment to responsible data in the UK's National Data Strategy could be realised and what it misses.
Participatory data governance
Enabling a participatory approach to data use, access, sharing and governance where beneficiaries can control and oversee the use of their data.
Tackling health and social inequalities in data-driven systems
Research to examine the interaction between data-driven systems and health and social inequalities, in the wake of COVID-19.
Boundaries of health data
Exploring how the datafication of health occurs and what consequences it has for people and society.
Who we work with
Opportunities for organisations and communities to collaborate with us.
The Citizens’ Biometrics Council
Bringing together 50 members of the UK public to deliberate on the use of biometrics technologies like facial recognition.
Creative Commons 4.0 licence
Content published by the Ada Lovelace Institute is shared under a CC-BY 4.0 license, unless otherwise stated.
The ethical case for data fiduciaries
Trust, vulnerability and trustworthiness, and ensuring that the interests of big tech are aligned with the interests of their users.
Data stewardship: an archival perspective
Archives as datasets? What can we learn from archivists in data preservation and sharing?
Strength in numbers: a case study for building a data-based community in cystic fibrosis
Now, more than ever, data can be used to bring people together as well as numbers.
Ada Lovelace Institute’s JUST AI network announces £40,000 AHRC support for projects addressing racial justice and AI ethics
Grants for projects designed to surface alternative, critical and diverse perspectives on data and AI in relation to racial justice.
Working with the CARE principles: operationalising Indigenous data governance
Shifting the focus of data governance from consultation to values-based relationships to promote equitable Indigenous participation in data processes.