Here's a look at some of the top regulatory stories for medical device companies this week: FDA wants another panel hearing on Boston Scientific's Watchman anti-stroke device; FDA talks Twitter and other online etiquette for medtech makers; Malaysian medical device market regulators clarify, expand policies; FDA issues draft guidances for industry on social media and internet communications about medical products: Designed with patients in mind; Scotland curbs use of transvaginal mesh amid global outcry.
FDA wants another panel hearing on Boston Scientific's Watchman anti-stroke device
June 17, 2014 by Brad Perriello
Boston Scientific, C.R. Bard, Emergo Group, European Commission, Food & Drug Administration (FDA), Johnson & Johnson, Medicines & Healthcare products Regulatory Agency (MHRA)
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