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If the NDI document is supposed to be about balancing safety vs access, it clearly errs way on the side of alleged safety -- I say alleged because supplements are among the safety category of products available to consumers today. This document seeks to re-interpret DSHEA. This was not the intent of Congress. Where's Orrin Hatch to call a hearing to tell the FDA what the intent of the law was since he's the one who essentially wrote it!</p>
Comment User:
Todd Runestad
