We are committed to quality; it is evident throughout every phase of product development, manufacturing and filling. As an FDA registered facility we continuously update knowledge relating to documented protocols, procedures, and ongoing personnel training. Absolute attention to every facet of the manufacturing process is ensured through regular internal and third-party audits. Our QC/QA department is involved with every aspect of our daily operation, working closely with our staff to provide ongoing training and quality awareness.

We are equipped to satisfy requirements for QC/QA and adhere to numerous testing and procedural protocols including those noted:

– Abide by protocols imposed by Federal and State agencies

– Total cGMP compliance

– Raw material analysis and evaluation

– Laboratory analysis of products

– Long term stability testing**

– Process and Methods Validation testing

– Microbiological testing

– Product/Package compatibility testing

**During the process of product development, we run stability tests along with other controls to ensure the efficacy of your approved formulation