Convene a meeting with key stakeholders and organizations including representatives from the All of Us Research Program (formerly the NIH Precision Medicine Initiative) to discuss policies for streamlining and innovating patient/participant consent and data sharing.
- Align guidelines for streamlined electronic consenting and other consenting models that give ownership of health care data to patients and study participants with All of Us and FDA.
- Research Implementation Area
- Recruitment and Citizen Engagement
- To Be Initiated