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The FDA recently gained more leverage over pharmaceutical companies. Will it use it?

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The U.S. Food and Drug Administration late last year got more leverage over pharmaceutical companies that received accelerated approvals for their drugs. How will the agency use its new powers?

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Not under the Biden administration.

Worked on TecentriqHCP startup in NSCLC for North America while at PPDCRO at the end of 2014. US_FDA approved it by 2019. Wrote so many reports for GO29436, 437, 537, 432, 431, 527 got RSI. PPD wrongfully terminated me 2017 after they injured fly_BUR in 2016. You’re welcome

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