PA... Do you think this would be good or bad for the industry?

Ceredumbellum

Member
Here's the link to the article. I hadn't heard of this before today. Curious what your thoughts on it are if it passes.
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I think it might help to get rid of all these grey market steroids. As for the other stuff, it shouldn't hurt, but if it requires gov't approval before being introduced to the market, that means delays... Perhaps long ones.
 
Ceredumbellum said:
Here's the link to the article. I hadn't heard of this before today. Curious what your thoughts on it are if it passes.
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I would need to see more details. Obviously the FDA doesnt have the manpower to read every label sent to them. However it would give them ammunition at hand if they were to have issues with any company

We all know mislabeling and misbranding is rampant in sports nutrition. To varying degrees this would be scary to many companies

It wouldnt really effect companies which spike their supps with stuff not on the label though
 
Beejis60 said:
I think it might help to get rid of all these grey market steroids. As for the other stuff, it shouldn't hurt, but if it requires gov't approval before being introduced to the market, that means delays... Perhaps long ones.
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this wouldnt involve govt approval

however the FDA often thinks many natural products are not dshea compliant. they think just about everything needs a new dietary ingredient notification, which requires tens of thousands of dollars of safety studies often.

its the NDIN requirements coupled with stuff like this labeling act thing that could really put an end to any innovation in the industry
 
If it doesn't stop companies from spiking products, it's just more worthless legislation
 
SBH said:
If it doesn't stop companies from spiking products, it's just more worthless legislation
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it would allow the FDA to screen for ingredients on the label that they believe dont qualify as supplements though
 
Patrick Arnold said:
this wouldnt involve govt approvalhowever the FDA often thinks many natural products are not dshea compliant. they think just about everything needs a new dietary ingredient notification, which requires tens of thousands of dollars of safety studies often. its the NDIN requirements coupled with stuff like this labeling act thing that could really put an end to any innovation in the industry
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I say it's bad then. The gov deciding what qualifies as supplementation. Should make more patients for Obamacare tho
 
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