All aseptic manipulations at NexGen Compounding Pharmacy are performed in ISO 5 class hoods inside ISO 7 class clean rooms equipped with High-Efficiency Particulate Air (HEPA). Our cleanrooms and laminar airflow hoods are certified every 6 months by an independent agency to ensure operational efficiency. Our facility also meets all applicable USP <795> and USP <797> guidelines.
Our systems are designed to minimize the risk of human error. Every chemical in our inventory is verified, bar coded and scanned into our pharmacy software prior to being used in the compounding process. Our equipment, including our scales, are connected to our pharmacy software and the weights of the chemicals being used in each compound is recorded.
If the weight of an individual chemical is out of acceptable limits, our software immediately warns the user and puts a halt to the compounding process.
Every formula has a written protocol and is followed for every preparation, ensuring consistency.
Each batch is assigned a unique lot number and is recorded electronically. This enables our staff to access detailed data about any of our lots, including dispensing data, so we can easily and efficiently identify which lot of a particular preparation was dispensed to a specific patient.