QuVa Pharma, Inc, a national platform for compounded sterile preparations (CSPs), offers a consistent, reliable supply and exceeds industry standards for sterility, endotoxin, and potency testing. End product testing is performed at the highest level by testing every batch, every time; a product is never released at-risk. A Certificate of Analysis accompanies every batch. QuVa Pharma has extensive experience in cGMP and aseptic pharmaceutical manufacturing, and meets or exceeds all recent FDA requirements around sterile compounding.