DrugLog® ready for launch in the US
Pharmacolog has registered DrugLog® with the US Food and Drug Administration (FDA) and can thereby sell and deliver systems to the US market.DrugLog® is used to verify the identity and concentration of injectable drugs prior to administration for increased patient safety and has been sold in Europe since 2017. The system is classified as a Class 1 Medical Device and has undergone special tests required for registration with the US Food and Drug Administration (FDA) in the North American market. With the registration with the FDA, the product is now approved for sale in the U.S. as well.