This consensus statement reflects the deliberations of an international group of stakeholders with a range of expertise in public involvement and engagement (PI&E) relating to data-intensive health research. It sets out eight key principles to establish a secure role for PI&E in and with the research community internationally and ensure best practice in its execution. Our aim is to promote culture change and societal benefits through ensuring a socially responsible trajectory for innovations in this field
Evidence-based sexual and reproductive health is a global endeavor without borders. Inter-sectorial ...
Rationale, aims and objectives Involving members of the public in health research is said to produc...
This paper is the work of the first cohort of the Farr Institute's “Future Leaders” scheme. The Futu...
This consensus statement reflects the deliberations of an international group of stakeholders with a...
Introduction Data-intensive health research is a fast moving field in which public involvement and e...
Funding Statement This project was funded by The Farr Institute of Health Informatics Research. The ...
BACKGROUND: Large-scale linkage of international clinical datasets could lead to unique insights int...
Objective: There is growing interest in the potential benefits of public involvement (PI) in health ...
The value of using population data to answer important questions for individual and societal benefit...
The last 6 years have seen sustained investment in health data science in the United Kingdom and bey...
Community and public engagement (CPE) is increasingly becoming a key component in global health rese...
Patient and public involvement (PPI) is inconsistently reported in health and social care research. ...
Information is increasingly digital, creating opportunities to respond to pressing issues about huma...
Research integrity and research fairness have gained considerable momentum in the past decade and ha...
Big Data hold great promise for scientific health research and healthcare. Yet data-intensive health...
Evidence-based sexual and reproductive health is a global endeavor without borders. Inter-sectorial ...
Rationale, aims and objectives Involving members of the public in health research is said to produc...
This paper is the work of the first cohort of the Farr Institute's “Future Leaders” scheme. The Futu...
This consensus statement reflects the deliberations of an international group of stakeholders with a...
Introduction Data-intensive health research is a fast moving field in which public involvement and e...
Funding Statement This project was funded by The Farr Institute of Health Informatics Research. The ...
BACKGROUND: Large-scale linkage of international clinical datasets could lead to unique insights int...
Objective: There is growing interest in the potential benefits of public involvement (PI) in health ...
The value of using population data to answer important questions for individual and societal benefit...
The last 6 years have seen sustained investment in health data science in the United Kingdom and bey...
Community and public engagement (CPE) is increasingly becoming a key component in global health rese...
Patient and public involvement (PPI) is inconsistently reported in health and social care research. ...
Information is increasingly digital, creating opportunities to respond to pressing issues about huma...
Research integrity and research fairness have gained considerable momentum in the past decade and ha...
Big Data hold great promise for scientific health research and healthcare. Yet data-intensive health...
Evidence-based sexual and reproductive health is a global endeavor without borders. Inter-sectorial ...
Rationale, aims and objectives Involving members of the public in health research is said to produc...
This paper is the work of the first cohort of the Farr Institute's “Future Leaders” scheme. The Futu...