Nearly a third of FDA medical device adverse event reports filed late
A study has found that nearly a third of medical device AEs were reported by manufacturers later than FDA's required 30-day window across three years. The post Nearly a third of FDA medical device adverse event reports filed late appeared first on Medical Device Network.
A study has found that nearly a third of medical device AEs were reported by manufacturers later than FDA's required 30-day window across three years.
The post Nearly a third of FDA medical device adverse event reports filed late appeared first on Medical Device Network.
