Increasing Diversity in Clinical Trials and Health Data
This act aims to boost participation of diverse groups in clinical trials, especially for COVID-19. It will make remote trials easier and ensure that medicines and therapies are better suited for all citizens, regardless of background or status. Additionally, it will improve health data collection, aiding better public health planning.
Key points
Facilitating remote participation in clinical trials (e.g., via telemedicine), increasing accessibility for people from various regions and backgrounds.
Encouraging participation in trials from racial and ethnic minorities, the elderly, and low-income populations to make study results more representative.
Allowing free provision of digital devices (e.g., smartphones) for trial participation, reducing financial barriers for participants.
Improving demographic data collection for COVID-19 to better understand the disease's impact on different social groups and plan aid more effectively.
Simplifying rules for compensation in clinical trials to encourage more people to participate.
Expired
Additional Information
Print number: 117_S_2706
Sponsor: Sen. Menendez, Robert [D-NJ]
Process start date: 2021-08-10