Commitment to Quality
Our end-to-end process strives to be consistent with current Good Manufacturing Practice (cGMP) as outlined in the FDA's guidelines for human cell and tissue products. Provia's quality management system is consistent with best practices in the industry.
We process cells in a Class 10,000 clean room. Provia's facilities are backed up with an emergency generator, secured by sophisticated monitoring systems, and protected against natural disasters.
Our processes are consistent with best practices stated in the AAPD Policy on Stem Cells and federal and state regulations.
Please note: Provia Laboratories, LLC.'s activities for New York State residents are limited to collection of teeth extracted from autogeneic donors. Provia Laboratories, LLC.'s possession of a New York State license for such collection does not indicate approval or endorsement of possible future uses or future suitability of dental pulp derived cells.