Regulation & policy

CRN updates vitamin K2 MK-7 intake limits

CRN updates vitamin K2 MK-7 intake limits

By Stephen Daniells

The Council for Responsible Nutrition (CRN) has determined a Highest Observed Intake (HOI) level for vitamin K2-MK7 of 375 mcg/day following a review of over 40 clinical trials.

HHS brings back NHANES staff for public health

News in brief

HHS brings back NHANES staff for public health

By Asia Sherman

The Department of Health and Human Services (HHS) has rescinded the reduction in force notices for staff involved with the National Health and Nutrition Examination Survey (NHANES) following public pressure to recognize the importance of the survey for...

規制レビュー:偽造品、成分不一致、NMNのステータス

規制レビュー:偽造品、成分不一致、NMNのステータス

By Hui Ling Dang

マレーシア企業Holista Colltechが自社オメガ3製品の偽造問題を受け規制当局への強い働きかけを要請、オーストラリア規制当局が輸入メラトニンサプリメントの成分不一致を指摘、米国FDAがNMNのサプリメントとしての合法性を宣言―規制関連ニュースの最新動向をまとめました。

Michigan legislator introduces restrictive supplements bill

Michigan legislator introduces restrictive supplements bill

By Stephen Daniells

A lawmaker in Michigan has filed a bill to prohibit the sale of weight loss and muscle building products to minors. The Council for Responsible Nutrition said the bill is “premised on a misunderstanding of both the science and the regulation of dietary...

EFSA sets safe limit for Delta-8 THC

EFSA sets safe limit for Delta-8 THC

By Nikki Hancocks

The European Food Safety Authority (EFSA) has suggested a safe limit of 1 µg/kg body weight for the combined intake of delta-8 and delta-9 THC from food.

监管审查:假冒产品、含量不符、 NMN 合法化

监管审查:假冒产品、含量不符、 NMN 合法化

By Hui Ling Dang

本期监管动态为您带来最新进展,包括马来西亚公司 Holista Colltech 因旗下 Omega-3 产品遭遇假冒问题呼吁行业加强与监管机构沟通、澳大利亚监管机构警示进口褪黑素补充剂含量不符问题、美国 FDA 宣布 NMN 可作为膳食补充剂合法使用。

CHPA’s MacKay on growth, challenges, MAHA and going mainstream

CHPA’s MacKay on growth, challenges, MAHA and going mainstream

By Danielle Masterson

The Dietary Supplement Health and Education Act (DSHEA) was signed into law in 1994 by President Bill Clinton, creating the modern dietary supplements industry as we know it. When DSHEA passed, the industry had 4K products and was worth $4 billion....

CRN’s Mister on the regulatory curveball nobody saw coming

CRN’s Mister on the regulatory curveball nobody saw coming

By Danielle Masterson

The Trump Administration returned to the White House one year ago. From Robert F. Kennedy Jr. being named health secretary, to tariffs, to Make America Healthy Again, it’s been an eventful year for a variety of sectors—including dietary supplements.

ANH pushes FDA to broaden access to medical foods

ANH pushes FDA to broaden access to medical foods

By Ben Hargreaves

The Alliance for Natural Health (ANH) USA is calling for FDA regulatory reform to broaden access to medical foods, with the aim of using nutrition therapies to help manage chronic disease and other conditions.

UNPA’s Israelsen on the work behind an ODI 2.0 list

UNPA’s Israelsen on the work behind an ODI 2.0 list

By Stephen Daniells

With new information about how FDA views key dates with drug preclusion and efforts to eradicate self-affirmed GRAS, it is time to revisit the list of pre-DSHEA or old dietary ingredients (ODI), says Loren Israelsen, founder and president of the United...

Fabricant on government shutdown, NMN and 90 years of NPA

Fabricant on government shutdown, NMN and 90 years of NPA

By Stephen Daniells

The ongoing government shutdown is impacting GMP inspections and delaying proposals to amend the Generally Recognized as Safe (GRAS) regulation. “We’re gonna just sit on our hands for a little while longer,” says Dr. Daniel Fabricant, president and CEO...

Is kratom tarnishing kava’s reputation?

Is kratom tarnishing kava’s reputation?

By Danielle Masterson

Consumer priorities have undergone a major shift in recent years, with mental wellness emerging as a top concern. Given the focus on mental health, it may not be surprising that demand for functional beverages like kava are on the rise.

Supplements 101: Understanding European health claims

Supplements 101: Understanding European health claims

By Lauren Nicolle

The European dietary supplement regulatory system can seem complex and difficult to navigate. Here, NutraIngredients+ breaks down the answers to some of the most commonly asked regulatory questions with insights from leading experts in the field.

Q&A: Supplement brands face new AI decision-making rules

Q&A: Supplement brands face new AI decision-making rules

By Cassandra Stern

The California Consumer Privacy Act (CCPA) has implications for dietary supplement stakeholders. In this Q&A, Nikki Bhargava, a partner in the Emerging Technologies group at global law firm Reed Smith breaks down what you need to know.

‘A pivotal expansion’: European inulin producers join IPA

‘A pivotal expansion’: European inulin producers join IPA

By Stephen Daniells

The European Association of Chicory Inulin Producers (CEFI) has joined the International Probiotics Association, a move that IPA calls “a pivotal expansion in the representation of prebiotic science and industry worldwide”.

Dietary supplements no longer included in AB 899

Dietary supplements no longer included in AB 899

By Danielle Masterson

After going back and forth with CA lawmakers over whether supplements are included in the legislation, CRN reports that it has secured clarifying language with the enactment of SB 862.

IPA opens China office, unveils upcoming plans

Vitafoods Asia 2025

IPA opens China office, unveils upcoming plans

By Tingmin Koe

The International Probiotics Association (IPA) has officially opened its China office located in Shanghai, and Executive Director George Paraskevakos recently spoke with NutraIngredients on the association’s plans in the country.

The ‘proteinification’ of everything

The ‘proteinification’ of everything

By Danielle Masterson

Once just a bottle shaker staple, protein is taking on new forms and finding its way into everything from soda to chips to macaroni and cheese.

FDA declares NMN lawful in dietary supplements

FDA declares NMN lawful in dietary supplements

By Stephen Daniells

The U.S. Food and Drug Administration (FDA) has responded to a Citizen Petition from the Natural Products Association (NPA) and the Alliance for Natural Health USA (ANH) on the status of NMN, declaring the vitamin B3 form to be lawful for use in dietary...