Rebecca Wright12.01.10
“With GMPs squarely upon us, this is the industry’s chance to shine. It should be every company’s duty to make sure it is meeting and in some cases exceeding these requirements. The same goes for adverse event reporting.
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“Regulations across the globe will take on new significance in 2011. European health authorities are already impacting the industry in a major way, and the U.S. may not be far behind. At the same time, regulations are in the embryonic stages in many of the developing regions for dietary supplements and functional foods (Brazil, Russia, India, China). If you want in on any of these markets, get to know the authorities there.
“Research might be one of the biggest game-changers in the near future. It will not only be necessary to prove product effectiveness, but also to confirm safety, so start planning your clinical studies now.
“As for healthcare, it is the industry’s job to make consumers understand how important dietary supplements and functional foods are to their daily wellness routines. Once they realize that o
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