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Article claims FDA “provides scant oversight” in medical device monitoring
  • Shook Hardy & Bacon LLP
  • USA
  • November 11 2010

According to a recent article on the effectiveness of post-market surveillance, medical device manufacturers "often fail to properly conduct safety studies" and the Food and Drug Administration (FDA) "provides scant oversight" in post-approval monitoring of these devices.

Greg Fowler
  • Shook Hardy & Bacon LLP