Scaling Up Your Methods With USP <621> - Part 1: Chemistry

Whether you are a scientist doing liquid chromatography in the pharmaceutical, food, or supplement industry, you want to ensure the safety and quality of your products. To improve global health through consistent public standards, the United States Pharmacopeia developed USP <621>, a quality standard for the drug development industry, used to define terms and procedures used in chromatography, including allowable adjustments for methods.

Explore the revised USP <621> guidelines that are scheduled to take effect in the near future. These critical updates to USP <621> involve changes to the allowable modifications to gradients.