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Food Safety Modernization Act


OmniActive’s Facilities Achieve NSF-GMP Certification

by Shari Barbanel | August 18, 2025

OmniActive Health Technologies (Mumbai, India, and Bridgewater, NJ) has announced that both its manufacturing facilities in Pune and Hosur, India have achieved good manufacturing practice (GMP) compliance certification from NSF International. The certification was awarded under NSF/ANSI 173, Section 8, which includes requirements from the Food Safety Modernization Act (FSMA) and current good manufacturing practices ...

ProTab Labs Offers Solutions for Infant Formula Producers Facing Crisis

by Shari Barbanel | June 22, 2022

To tackle the infant formula crisis, producers can rely on Southern California supplement solutions contract manufacturer ProTab Laboratories to blend custom premixes and produce and package infant formula with a rapid turnaround time, the company stated. “ProTab is in the perfect position as a supplement solution manufacturer and packager to prioritize infant formula production with safety and ...

Natural Ingredient Suppliers and Manufacturers Adjust to COVID-19 Fight

by Shari Barbanel | March 24, 2020

With the number of cases of the Coronavirus (COVID-19) growing by the day and a number of states enforcing “shelter-in-place” orders, natural product manufacturers and ingredient suppliers are adjusting their practices to meet the new realities of working during a pandemic. Guidance from the Department of Homeland Security (DHS), and President Trump’s declaration that workers ...

Food & Beverage Issue Alliance Requests FDA Enforcement Discretion for New Nutrition Labeling Rule

by Shari Barbanel | October 8, 2019

The American Herbal Products Association (AHPA) has joined 12 leading trade associations to advocate FDA (U.S. Food and Drug Administration) to provide flexibility in its enforcement of the new nutrition labeling rules as the January 1, 2020 compliance date approaches. In a letter to Acting FDA Commissioner Dr. Ned Sharpless, the associations, acting as the ...

USP Announces Updated Ingredient Verification Program

by Shari Barbanel | April 23, 2018

USP (United States Pharmacopeia) has updated its Ingredient Verification Programs (IVP), services that help companies ensure they meet quality standards for ingredients used in the manufacture of dietary supplements and drug products. USP has IVPs for dietary ingredients (IVP-DI), for excipients (IVP-E) and for active pharmaceutical ingredients (IVP-API). Manufacturers of finished dietary supplements and drug ...

Senator Hatch Announces Retirement

by Shari Barbanel | January 3, 2018

On January 2, the longest-serving Senate Republican, Senator Orrin Hatch of Utah announced that he would not seek re-election for an eighth term. Sen. Hatch, who formed and led the Dietary Supplement Caucus in the Senate, co-authored the landmark legislation that established a rational framework for regulating dietary supplements, the Dietary Supplement Health and Education ...

Registrar Corp Introduces FDA Compliance Monitor

by Shari Barbanel | January 12, 2016

The U.S. Food and Drug Administration (FDA) recently finalized two new rules that require food facilities and importers of food and beverages to monitor and document the compliance status of each supplier, “including FDA warning letters or import alerts relating to the safety of food and other FDA compliance actions.” The two new rules, the Preventive ...

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