LIAVITA’s state-of-the-art NSF/ANSI Standard 173, Section 8 Good Manufacturing Practice (GMP) Certified facility, bring high quality raw, bulk and finished US Products to our customers worldwide. Few decisions are as critical as selecting the right GMP partner for your dietary supplement raw material needs.  Raw material manufactured to GMP standards for commercial sale must meet requirements for identity, strength, quality and purity.

• FDA, EDQM, and TGA
• GMP for API and GMP compliance for final products
• ISO14001 Environmental Management System certification
• Parenteral drug formulation R&D lab with GLP standard
• GLP Analytical R&D lab
• GLP QC lab
• Good QA and EHS system
• BRC Certified