When you buy reference standards, you want the best possible support in quality control. USP Reference Standards are founded on a robust, collaborative scientific process unlike any other and are rigorously tested in laboratories around the globe.
In a recent perception survey, generic drug manufacturers responded that using pharmacopeial reference standards accelerated product development and reduced the risk of ANDA rejection. Specifically, your peers reported:
- Average formulation time reduced by 26%
- Method development time reduced by 31%
- Validation time reduced by 29%
- Total product development time reduced by 19%
Order from our 2020 catalog of highly characterized USP Reference Standards and documentation to benefit from the industry benchmark trusted in more than 140 countries. Need help? Access our global customer service, in-house scientific experts, and other resources to make your work even more efficient and cost-effective.