date:Jun 01, 2012
ent to the pending Food and Drug Administration (FDA) User Fee Act to require dietary supplement facility registration and product listing.
The industry grassroots were scrambled, and the Big 5 trade associations mobilized their Capitol Hill champions andthe amendment was tabled to a chorus of cheers from the industry.
Remove all doubts about safety and arguments about energy shots and adulteration fall silent.
If a company cannot comply with GMPs with its internal resources and infrastructur