Reinvigorating nondelegation requires not just a reformulation of the doctrine, but also a willingness to apply it.

In response, the U.S. Congress passed the Federal Food, Drug and Cosmetic Act of 1938, granting FDA with “premarket review” ...

A federal consumer protection agency's withdrawal of numerous guidance documents will have little legal effect.

Today, as Penn Carey Law celebrates the entire Class of 2025, The Regulatory Review is pleased to share this special ...

Feldman and Schor explain that the patent dance is a complex process to determine which of a biologic manufacturer’s patents ...

As the United States braces for what is likely to be another record-setting hurricane and wildfire season, one critical issue ...

In a conversation with The Regulatory Review, public health expert Mitch Zeller reflects on his tenure at the U.S. Food and ...

President Trump signed four Congressional Review Act resolutions into law, repealing Biden-era regulations on energy ...

UN advisory body evaluates opportunities for the international regulation of artificial intelligence. The HLAB argues that AI has the potential to be used for good, raising biomedical research and ...

When an agency issues or repeals a rule, it must undergo a set of procedures laid out in the Administrative Procedure Act (APA). Among these procedures is notice and comment, which involves notifying ...