From 9/11 to COVID-19: A Brief History of FDA Emergency Use Authorization
The history of EUA involves fundamental questions about the role of public officials, scientific expertise, and administrative norms in times of crisis.

The history of EUA involves fundamental questions about the role of public officials, scientific expertise, and administrative norms in times of crisis.

We explain why COVID-19 vaccines are only just starting to be tested in children and what policymakers can do to spur pediatric vaccine trials.

This blog post provides an overview of the FDA’s emergency authorization powers and analyzes the extent of their usage in the COVID-19 pandemic.

Pharmaceutical companies are now also engaging the public themselves in an attempt to build trust in their products.

Moderna’s vaccine works using a completely novel mechanism, unlike any other vaccine currently approved anywhere in the world.

No vaccine for the novel coronavirus has been approved. Nevertheless, governments and organizations are making deals for tens of millions of doses.

It remains to be seen whether Congress or the Administration adopt more decisive measures toward the control of drug prices than they have in the past.

As the search for COVID-19 treatments and vaccines continues, questions of pricing and access are beginning to emerge.

With the sudden spike in hospitalized patients with COVID-19 symptoms, physicians are using these drugs faster than manufacturers are making them.
