Regulation

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Guest article

NPA: Setting safety limit on CBD key part of regulatory process

By Daniel Fabricant, PhD, Natural Products Association

NPA president and CEO Daniel Fabricant, PhD, argues that FDA does not need new authorities to regulate the CBD market and that determining a safe daily intake level for the substance should be an integral part of that process.

NJ Labs: “ISO accreditation is not enough”

NJ Labs: “ISO accreditation is not enough”

By Danielle Masterson

Amazon heightened the priority of ISO/IEC 17025:2017 when it announced to dietary supplement sellers that ISO accreditation is required, along with Current Good Manufacturing Practice (CGMP) in order to sell products on its online retail platform.

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Guest article

CRN: Don’t Sell Out DSHEA for CBD

By By Steve Mister, President & CEO, Council for Responsible Nutrition

We all want an expedient solution to the stalemate with FDA over the legal status of cannabidiol (CBD), but the call to allow FDA to set a maximum safe level for CBD is antithetical to the law governing dietary supplements, DSHEA.

Industry reunites at SupplySide East

Industry reunites at SupplySide East

By Danielle Masterson

Excitement was high in Secaucus, NJ as the supplement industry gathered again in person following nearly two years of zoom calls.

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NPA files petition asking FDA to rule NAC as legal ingredient

By Hank Schultz

The Natural Products Association has filed a citizen’s petition asking FDA to acknowledge NAC as a legal dietary ingredient. The molecule, which has been on the market for decades, was ruled last year as violative by the Agency.

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