Are the NDI guidelines the ultimate FDA tool to freeze dietary supplement innovation? A special report by Robert Verkerk, PhD, ANH-USA Scientific Director and ANH-Europe Executive and Scientific Director.
The FDA is trying to turn a simple notification system for new supplements into a totally arbitrary approval system. Let’s tell the FDA that supplements are not drugs and ask Congress for help!
Sen. Durbin’s disingenuous “Dietary Supplement Labeling Act,” which we told you about last week, needs to be defeated. This week we explain why in greater depth. Tell your senators!
Just before the July 4 holiday weekend, hoping to limit media attention, the FDA dropped a bomb on dietary supplements. Don’t let them get away with it! A new Action Alert.
This new bill pretends to be consumer-oriented but will give the FDA new powers it could easily misuse, restricting your access to supplements and raising the cost of buying them. An important new Action Alert for Congress!
Today, both the FDA and Sen. Dick Durbin (D-IL) dropped policy “bombs” on those of us who use dietary supplements. By timing the introduction of their anti-supplement legislation and regulatory guidance to be released before a holiday weekend, the FDA and Sen. Durbin are both hoping to evade negative publicity.
Senator Durbin’s bill, which will be introduced in Congress this week, is likely to be another example of burdensome and unnecessary legislation.
Melatonin-filled brownies called Lazy Cakes have come to the attention of Congress. Will the FDA use them as another excuse to over-regulate dietary supplements?
Misleading claims vs. legitimate science—getting to the truth can be a minefield! Which is why the Free Speech about Science Act is so important.
We know that the FDA is discussing new regulatory requirements for supplements.