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Congress


NPA Responds as Durbin-Braun Proposal for Dietary Supplements Makes Its Way into PDUFA

by Angela Sabarese | May 23, 2022

On May 17, the United States Senate Health, Education, Labor, and Pensions Committee (HELP) released a discussion draft of its legislation to reauthorize FDA user fees for drugs, biologics and medical devices package, which includes the controversial and divisive Durbin-Braun premarket approval concept and more that would be damaging to the industry, according to the ...

NPA Applauds House Energy & Commerce Committee for Excluding Dietary Supplements from User-fee Reauthorization Legislative Package

by Angela Sabarese | May 9, 2022

On May 4, the United States House of Representatives Energy and Commerce Committee unveiled its FDA User Fee legislative package, which did not include the “mandatory product listing” concept in its legislation to reauthorize FDA user fees for drugs, biologics and medical devices. “The NPA applauds Chairman Frank Pallone and Republican Leader Cathy McMorris Rodgers ...

NPA Says Mandatory Product Listing is a “Non-Starter” and Amounts to “Pre-Market Approval”

by Angela Sabarese | April 5, 2022

The Natural Products Association (NPA) has issued a statement on the President’s FY 2023 Budget Request to Congress regarding the section on the U.S. Food and Drug Administration (FDA). “FDA’s proposal to include mandatory product listing in their FY23 budget request is a non-starter,” said Dr. Daniel Fabricant, the association’s president and CEO. “Year after ...

Bipartisan Legislation to Regulate Hemp-derived CBD Re-introduced in Congress

by Angela Sabarese | February 8, 2021

On Feb. 4, 2021 Representative Kurt Schrader (D-OR) and Representative Morgan Griffith (R-VA) re-introduced bipartisan legislation that would protect public health by providing legal clarity in the cannabidiol (CBD) product marketplace. Re-introduced in the 117th Congress as HR 841, the Hemp and Hemp-derived CBD Consumer Protection and Market Stabilization Act of 2021 directs the U.S. ...

Congressional Staff Educated on Dietary Supplements’ Role in Immune Health

by Angela Sabarese | December 16, 2020

Tieraona Low Dog, M.D., recently educated congressional staffers on the responsible role of dietary supplements in supporting immune health, as well as their many other health and wellness benefits, particularly in the era of COVID-19. Low Dog was featured at the final Congressional Dietary Supplement Caucus (DSC) briefing of 2020, held last week. An expert ...

NPA Joins Coalition to Push Congress to Include Tax Credit in Stimulus Package

by Nicholas Saraceno | August 18, 2020

As Congress continues deliberations on additional financial assistance for individuals and companies impacted by the pandemic, the Natural Products Association (NPA) is joining businesses representing millions of workers and customers in an open letter asking officials to include tax credits for businesses facing steep reopening costs, as noted previously. Most recently however, a letter to ...

FDA Submits CBD Enforcement Guidance to White House For Review

by Nicholas Saraceno | July 27, 2020

U.S. Food and Drug Administration (FDA) has submitted draft CBD (cannabidiol) enforcement guidance to the White House Office of Management and Budget (OMB) for review, according to Marijuana Moment. The contents or even basic scope of the document titled, “Cannabidiol Enforcement Policy; Draft Guidance for Industry,” are not yet publicly known. The agency was mandated ...

NPA Survey: Natural Products Businesses Brace for Big Reopening Bills

by Nicholas Saraceno | July 27, 2020

As Congress begins deliberations on additional financial assistance for individuals and companies impacted by the pandemic, the Natural Products Association (NPA) is pushing officials to include tax credits for natural products businesses facing steep reopening costs. In a new survey, NPA members projected spending an annual average of $13,595—with some expected to spend as much as $200,000—on ...

Hawaii Becomes Third State to Propose CBD Regulations

by Nicholas Saraceno | July 14, 2020

As the Food and Drug Administration (FDA) continues to defy mounting requests from the U.S. Congress and the natural products industry to provide science-based and public health regulations for CBD, more states are rushing in to fill the vacuum. The State of Hawaii recently joined Virginia and Texas in proposing new state regulations for consumable hemp ...

FDA’s CBD Report to Congress Underscores Need for Regulations

by Nicholas Saraceno | July 14, 2020

While the U.S. Food and Drug Administration (FDA) has been tasked with regulating the cannabidiol (CBD) industry, the agency has repeatedly asserted it will not do so until it receives sufficient data on the cannabinoid’s safety for consumers. Yet, according to HempGrower, the agency’s latest report to Congress on July 8 evaluating the CBD marketplace underscores ...

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