The facility offers full contract manufacturing capabilities, including blending, tableting and encapusulation. The facility also has in-house quality control labs covering analytical, chemical and microbiological testing to assure finished goods meet the highest standards. Inclusive are state-of-the-art stability chambers to allow for product stability testing in real time and accelerated conditions.
Earning GMP registration from NSF International verifies that Sabinsa’s Payson facility has the proper methods, equipment, facilities, and controls in place for producing dietary supplement products. NSF GMPs were developed in accordance with the U.S. Food and Drug Administration’s (FDA) 21 CFR part 111 regulation for dietary supplement manufacturing, packaging, and distribution.
“Although we have been GMP compliant for a number of years, we felt that third party facility registration through NSF provided our customers with additional peace of mind,”said Sabinsa Marketing Director Shaheen Majeed.
“As the variables in the QA programs of contract manufacturers becomes more pronounced, Sabinsa's earning NSF GMP registration for their Payson, Utah facility is a clear indication to customers and supply chain partners of their commitment to quality and safety," said Ed Wyszumiala, general manager of NSF International’s dietary supplement programs.