For more than 30 years our manufacturing facility, located in Atlanta, Georgia, USA, has been producing high-quality products for our customers.
AMVILAB is a licensed, FDA approved, and certified Current Good Manufacturing Practices manufacturer. AMVILAB is privately owned and operated.
AMVILAB's new facility is capable of manufacturing minimum custom runs as low as 25,000 capsules and capable of handling 1,000,000 capsule runs on a daily basis.
We also custom formulate and develop new formulas to stay in sync with the ongoing changes in the marketplace.
All AMVILAB products are FDA registered. All manufacturing takes place here in the United States at FDA registered manufacturing facilities that prepare our products conform to United States Pharmacopeia (USP) standards.
Pharmaceutical GMP - (Good Manufacturing Practice). GMP is concerned with both production and quality control. It ensures that pharmaceuticals are consistently produced and controlled to the quality standards appropriate to their intended use and as required by the product specification.
Amvilab manufacture sites operate to ISO 29002, or ISO 9001-2000. The International Organization for Standardization is a worldwide federation of national standards bodies from more than 140 countries. Their standards help increase the reliability and effectiveness of materials, products, processes and services.