Pharmaceutical Impurity Reference Standards are an essential part of ensuring the quality of pharmaceutical products.
What should I know about this?
They provide a way to measure and control impurities in pharmaceutical products and help to ensure that products meet regulatory requirements. Impurity Standards are available from a variety of sources, including commercial suppliers, academic institutions, and government agencies.
These Standards can be used to monitor the levels of impurities in finished products, raw materials, and intermediates. They can also be used to assess the purity of new synthetic routes or processes. These Standards are typically supplied as dry powders or liquids. Some standards are supplied as ready-to-use solutions, while others require dilution or other preparation prior to use.
What are the benefits of this?
It can help to ensure that products meet regulatory requirements. They can also help to improve the quality of pharmaceuticals and increase process efficiency.
We hope this information has been useful to you.