FSMA
OmniActive’s Facilities Achieve NSF-GMP Certification
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
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
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
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 ...
Embracing Botanical Extracts
While the popularity of certain medicinal plants may ebb and flow, the need for research and clean ingredients remains steady for botanical extracts in finished products. The National Institutes of Health’s Office of Dietary Supplements sums up a botanical best in its definition of the item—“a plant or plant part valued for its medicinal or ...
USP Announces Updated Ingredient Verification Program
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 ...
SIDI Work Group Calls for Comments on Draft of Updated Protocol
The dietary supplement industry’s self-regulatory coalition, the SIDI Work Group, recently released an updated draft of the “Standardized Information on Dietary Ingredients (SIDI) Protocol,” and seeks feedback from industry stakeholders and regulators by July 3, 2017. The SIDI Protocol has gained significant traction within the industry since its original release in 2008. The protocol provides ...
Registrar Corp Introduces FDA Compliance Monitor
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 ...
Industry Forecast
The participants are: • Dr. Daniel Fabricant, CEO & Executive Director, Natural Products Association, Washington, DC, (202) 223-0101 • Marcia S. Moll, Marketing Director, Dietary Supplements & Herbal Medicines, U.S. Pharmacopeia, Rockville, MD, (301) 881-0666 • George Pontiakos, President & CEO, BI Nutraceuticals, Rancho Dominguez, CA, (310) 669-2100 • Elan M. Sudberg, CEO Alkemist Labs, ...
Focus On Food Safety
NIE discusses the implications posed by FSMA with industry representatives, and their work to meet the challenges head on.In 2007, the U.S. Food and Drug Administration (FDA) published a “Final Rule,” establishing FDA regulations, which require current good manufacturing practices (cGMP) for dietary supplements (21 CFR 111). The final rule addresses in particular the identity, ...
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