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Lallemand Receives USP’s GMP Certificate for Canadian Production Facilities
Lallemand Health Solutions announced that both of its Canadian probiotic production plants in Montreal and Mirabel successfully passed the United States Pharmacopeia (USP) Quality Systems Good Manufacturing Practice (GMP) audit. The company thus has become the first probiotic production facilities to receive this quality certificate. “Such achievement illustrates our long-standing commitment to quality and demonstrates ...
TSI Group Invests in Transparent Botanical Production Platform
Hong Kong-based TSI Group Co., Ltd. (TSI) recently announced the creation of a new botanical products growing and manufacturing platform located in Yancheng, Jiangsu Province, China. The new venture is intended to elevate TSI’s manufacturing capabilities into a completely integrated “farm-to-product” growing and production platform that addresses today’s pressing market demands for authenticated botanical products ...
NPA and UL Partner for Expanded Industry Education
The Natural Products Association (NPA) and UL, a leading global independent safety science company, are working together to offer increased educational opportunities to NPA members. The education provided through joint NPA and UL efforts will provide online and in-person education for NPA members. The new education partnership, which will incorporate NPA’s prestigious regulatory and compliance seminars, ...
New FDA Inspection Tips from AHPA
The American Herbal Products Association’s (AHPA) teleseminar played a large role in helping the dietary supplement industry recognize and observe good manufacturing practices. The two-hour teleseminar, held in the middle of May, had industry legal experts, including Justin Prochnow, Esq, Marc Ullman, Esq and Ashish R. Talati, Esq provide pertinent tips on U.S. Food and ...
Preparing For An FDA Audit
NIE highlights the resources available and pitfalls to avoid so companies are completely prepared when an inspector comes knocking.In June 2007, the United States Food and Drug Administration (FDA) issued the Dietary Supplement Current Good Manufacturing Practice (cGMP) Final Rule 21 CFR Part 111. In essence, the final rule requires that the proper controls be ...
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