Engendering Equity in Biomedical Research by Meeting Communities Where They Are
What if researchers took more time to harness their power and training to elevate and mobilize the voices of the communities they study?

What if researchers took more time to harness their power and training to elevate and mobilize the voices of the communities they study?

Should consumers have access to the data that are collected via direct-to-consumer health apps? What real-world challenges might this create?

Direct-to-consumer health apps provide a window into key issues in the world of digital health. In this post, respondents consider data privacy concerns.

Contribute to the 2022 Petrie-Flom Center Annual Conference and subsequent book project!

Interesting empirical studies, policy analyses, and editorials on health law and policy issues from the month of April 2021.

As digital health products proliferate, entities that fall outside HIPAA regulation are collecting vast amounts of biometric information.

While moving too quickly with new technologies carries ethical and societal risks, moving too slowly could leave vulnerable people behind.

What obligations do researchers have to disclose potentially life-altering incidental findings as they happen in real time?

Obtaining voluntary competent informed consent is a critical aspect to conducting ethical deep phenotyping research.

Can intended parents who enter into a surrogacy contract change their mind once a pregnancy is already progressing?
