DSHEA transformed the dietary supplement industry in 1994. Today, Organic & Natural Health's Karen Howard calls for modernization to improve transparency, strengthen oversight, create national regulatory consistency, and support innovation. Here's what's being proposed.

A decades-old definition is under the microscope as FDA gathers input on dietary supplement ingredients and innovation.

Blaming DSHEA for “gas station drugs” misses the real issue: enforcement gaps, not lack of laws, according to a dietary supplement industry perspective.

Congressional hearings, Supreme Court challenges, FDA petitions, and new state food-labeling proposals are intensifying action over supplement oversight, health claims, and consumer transparency.

This is how you can help update the meaning of the dietary ingredient categories as defined in the Dietary Supplement Health and Education Act of 1994 (DSHEA).

Described as “much-needed reform around claims language, drug preclusion, and federal supremacy clause reform to forestall state-by-state regulation over supplements,” take a look at “DSHEA 10.0.”

FDA said the public meeting will help inform the agency's next steps regarding the meaning of the dietary supplement ingredient categories defined in DSHEA.

In addition to calling out now-discredited research, AHPA refuted repeated claims  that dietary supplements are "not well regulated" by FDA.

ANH-USA, CRN, and NPA share viewpoints on key issues impacting the natural products industry.

The 11th annual Organic & Natural Health Association conference celebrated members from the natural products industry while discussing ideas regarding current and future affairs.