We at NexGen understand that quality control within the pharmaceutical industry is of paramount importance, and this is doubly true in the area of pharmaceutical compounding. As experts in medication delivery, our pharmacists play an integral role in maintaining quality assurance and avoiding errors. Pharmacists at NexGen have a core knowledge of medications, including their adverse effects, interactions, proper dosing, and monitoring parameters. While our safety protocols are written to exacting standards, pharmacists at NexGen understand that it is equally important to work with ingredients and supplies of only the highest quality.

Standards set by the USP (see below) are also integrated into NexGen Pharmaceuticals' compounding practices.

At NexGen Pharmaceuticals, all our compounded medications meet and exceed all applicable USP standards. We perform internal sterility testing using dual media per USP guidelines as well as endotoxin testing in accordance with USP guidelines on each batch.

Additionally, all of the ingredients we use in our compounded preparations are determined to be stable, compatible, and appropriate for use according to USP guidelines. Certificates of Analysis are received from the manufacturer and verified for all the ingredients used in our preparations.

At NexGen, there is no compromise where standards are concerned, giving you the assurance that you're receiving the highest-quality compounded medication for your patients or animals.

What is USP?

The United States Pharmacopeial Convention (USP) is a nonprofit organization, that develops and publishes quality standards for medicines. Sterile and non-sterile compounding are covered under USP and USP , which detail best practices for compounding of prescription drugs.