06.03.19
INDIA: The Sami-Sabinsa Group’s Nelamangala biotechnology site in Bengaluru, India has been audited by the US Pharmacopeia (USP) and received a GMP compliance certificate. This site produces Sabinsa’s probiotics, enzyme blends as well as supercritical fluid extraction of various botanicals.
The certificate recognizes that the site operates GMP quality systems which meet the requirements set forth in 21 CFR Part 117 Current Good Manufacturing Practice, Hazard Analysis and Risk-Based Preventive Controls for Human Food, and USP-NF General Chapter Manufacturing Practices for Dietary Supplements for Dietary Ingredient Manufacturing.
“All of our facilities have undergone many inspections and certifications through the years and will continue to do so,” said Sabinsa founder Dr. Muhammed Majeed. “While we always encourage customers to visit us in India and see our five manufacturing facilities for themselves, we realize that’s not possible for everyone. Participating in the USP GMP audit program is another way we can assure customers of our steadfast commitment to producing quality ingredients. Our other facilities are scheduled for USP auditing in the near future.”
“USP is pleased to recognize Sabinsa’s successful completion of the USP Quality Systems GMP Audit Program for this site,” added John Atwater, senior director of USP Verification Services.
The certificate recognizes that the site operates GMP quality systems which meet the requirements set forth in 21 CFR Part 117 Current Good Manufacturing Practice, Hazard Analysis and Risk-Based Preventive Controls for Human Food, and USP-NF General Chapter Manufacturing Practices for Dietary Supplements for Dietary Ingredient Manufacturing.
“All of our facilities have undergone many inspections and certifications through the years and will continue to do so,” said Sabinsa founder Dr. Muhammed Majeed. “While we always encourage customers to visit us in India and see our five manufacturing facilities for themselves, we realize that’s not possible for everyone. Participating in the USP GMP audit program is another way we can assure customers of our steadfast commitment to producing quality ingredients. Our other facilities are scheduled for USP auditing in the near future.”
“USP is pleased to recognize Sabinsa’s successful completion of the USP Quality Systems GMP Audit Program for this site,” added John Atwater, senior director of USP Verification Services.
