From: Consent as a compositional act – a framework that provides clarity for the retention and use of data
data subject | A person over 18 years | Person under 18 years | legal representative | collective | Person under government custody | Person who self-identify as ethic minority | Person with difficulties processing information | |
Consent to | Goals | To advance science | To do research in any area | Improving health systems | For research, public benefit | For profit-driven research | ||
Action | Donate my health data | Donate social context data | Donate tissue and extracted data from my tissue | Donate complementary data on this and future clinical research | Donate complementary data to this and future qualitative research | Donate all my data for secondary research use | ||
Benefits | For research, public benefit | To receive tailored advice | To improve care for me | To do disease research on the illnesses, I live with. | To improve care for others | To do research outside of health | For self-profit | |
Timeframes | Indefinitely | As long as I am alive | Until my next visit to a health setting | Until I revoke | As long as legislation does not change | for 5 years | Today | |
Risk | Low | Medium | Hight | |||||
Jurisdictions | Any jurisdiction | Supra national political organisation | Country of legal residence | Country of citizenship | Territories with the same or more protections | Jurisdiction with the same legislation within this country | This county | |
Agents | Health actors under Official collective authorities | under Official collective authorities | Private Education institutions | Any Official collective authorities | Private companies | Commons | Everybody |