FDA

FDA has published a draft guidance on new dietary ingredients notification master files

Apr 8, 2024

The U.S. Food and Drug Administration (FDA) published a draft guidance on the submission of new dietary ingredient notification (NDIN) master files. The

Nammex Files Citizen Petition Requesting FDA Actions on Mushroom Product Labeling

Jun 19, 2023

industry news dietary supplements united natural products alliance unpa

Dear Colleagues — North American Reishi, Ltd (Nammex) has filed a citizen petition with FDA requesting that the agency correct mislabeling of dietary

Supplement makers may get temporary reprieve from FDA inspections

Jan 13, 2022

Larisa Pavlick is quoted: “Within the UNPA family, we understand that most responsible and reputable companies will remain on course, and we will

UNPA Interview | John Atwater – Regulatory Consultant – Valuable Resource for UNPA Members

Aug 15, 2022

Loren introduces John Atwater as our primary regulatory consultant, a valuable resource for all UNPA Members. To learn more about how you can

UNPA NAC submission to FDA

Feb 17, 2022

Dear UNPA Colleagues: On January 25, 2022, we submitted comments to the FDA Office of Dietary Supplement Programs, via Ms. Cara Welch, and

UNPA’s Israelsen calls for resolution of NDI issue – NutraIngredients-USA.com

Apr 2, 2024

loren israelsen and stephen daniells discuss NDI and FDA

Loren urges the FDA to “move along as quickly as they can” to finalize any outstanding sections of the New Dietary Ingredient guidance.

What Does FDA’s Reorganization Mean for the Dietary Supplement Industry?

Feb 29, 2024

Loren Israelsen from the United Natural Products Alliance shares insight on how agency priorities might change and how businesses can prepare.

The U.S. Food and Drug Administration is in process of a massive reorganization designed to streamline operations within a unified Human Foods Program