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chmp meeting minutes, page-11

  1. BB44
    97 Posts.
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    27/02/14
    12:46
    Post #: 13058889
    Just wondering, how can a device fall under guidelines for a medicine?

    As far as i am aware, this current audit cannot change the determination that it is a device, therefore shouldn't all regulations regarding it fall under the device category?

    If that isn't the case, why even bother with categories??
    TIS Price at posting: 28.5¢ Sentiment: Hold Disclosure: Held
    Likes Created with Sketch. 1  Upvote
    lightbulb Created with Sketch.  Great analysis
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