Rebuilding Trust in Public Health and Public Health Law
As we rebuild trust in public health, we can begin to work toward reinstatement of public health law’s essential tools.

If public health is to prosper, we will need to overcome the after-effects of several failures of imagination.

Certain aspects of public health law as we know it are dead. In this symposium, we propose a path forward to create a “new public health” from the ashes.

The future of public health in an “RNA world” is on trial in a trade secrecy dispute worth $950 million.

Inefficiencies in negotiating vaccine procurement agreements during COVID-19 could have been attenuated with greater legal preparedness.

The use of fair, reasonable and non-discriminatory (“FRAND”) terms in the licensing of intellectual property rights could foster cooperation in pandemics.

Because of differences in how they were tested in clinical trials, it is difficult to make apples-to-apples comparisons for COVID-19 vaccines.

This post reflects on the ethical implications of FDA’s use of its emergency powers, and suggests opportunities for greater accountability moving forward.

A Biologics License Application, or BLA, is FDA’s standard “full approval” mechanism for biological products, including therapeutics and vaccines.
