MedPageToday
MedPage Today) — Among cardiovascular devices that were deemed unsafe enough to warrant urgent regulatory action, many had been allowed to skip rigorous premarket clinical testing in the first place, a report showed.
Researchers identified 137…
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Are Regulators the Root of the Problem of Serious Device Recalls?
Rebecka Fetzer
11:39
MedPage Today) — Among cardiovascular devices that were deemed unsafe enough to warrant urgent regulatory action, many had been allowed to skip rigorous premarket clinical testing in the first place, a report showed. Researchers identified 137…
