Here’s the latest news: Chinese city near North Korea partly shut on virus spreadElon Musk sues California county over shutdown Obama blasts Trump’s virus response as ‘chaotic disaster’ Our take on the latest developments U.S. regulators had to reverse themselves last week after moves to solve mask shortages and speed antibody tests to market backfired—a sign that even in a pandemic, it can pay for health officials to take their time. The Food and Drug Administration has been criticized in the past for being deliberate, and it was blamed for slowing the release of diagnostic tests in the early stages of the pandemic with needless bureaucracy. When Covid-19 began to spread in the U.S., it looked to remove some roadblocks. Now, the agency is undoing a mid-March policy that allowed antibody tests, which can tell whether someone has ever been infected with the new virus, to be sold without FDA review. The change opened the door for fraudulent tests that didn’t work like they claimed. Stephen Hahn, commissioner at the Food and Drug Administration since December. Photographer: Andrew Harrer/Bloomberg Similarly, the agency found N95 masks made in China that don’t provide proper protection. As a result, it reversed a policy change that allowed them on the market based on testing from third-party labs.
The conflict over whether FDA regulations hinder or help is an old one, but it’s been heightened during the Trump administration. For example, the president himself pushed Right to Try legislation backed by the libertarian Goldwater Institute in an effort to expand access to experimental drugs and forgo normal FDA protocols.
Vaping also fits in this category. Former FDA Commissioner Scott Gottlieb didn’t want the agency to potentially hinder a new technology, so pushed back FDA reviews of the products by several years. In the meantime, the U.S. experienced an epidemic of youth vaping.