Three Categories Of Pharmaceutical Impurity Reference Standards

The Pharmaceutical Impurity Reference Standards are a group of substances that can be used as references to test pharmaceutical products. Pharmaceutical impurities is the term given to any substance found in a drug that was not intentionally added but introduced during production or storage.

Pharmaceutical manufacturers need Pharmaceutical Impurity Reference Standards for testing and quality control purposes. These standards come in three categories: analytical, reference materials, and performance standards. To learn more about each category, read on!

This article discusses three types of Pharmaceutical Impurity Reference Standards:

-Analytical Pharmaceutical Impurity Reference Standard – this type of standard is used as an analytical tool by those who manufacture drugs; it’s obtained from a controlled process with uniform conditions.

-Reference Pharmaceutical Impurity Reference Standard – Pharmaceutical manufacturers, use this type of Pharmaceutical Impurity Reference Standard as reference material, and it’s made up of an already known substance.

-Performance Pharmaceutical Impurity Reference Standard – used by those who manufacture drugs for quality control purposes; manufactured in small quantities to ensure more accurate results.

Conclusion: Pharmaceutical Impurity Reference Standards are extremely important for Pharmaceutical manufacturers because they ensure accurate results, which means the drugs manufactured will be safe.

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