The world relies on pharmaceuticals, making it essential to uphold the highest standards of quality, safety, and efficacy in drug development.
Achieving this requires high accuracy and reliable analytical methods to measure and control the various attributes of the drug substances and products.
Among these analytical methods, two of the most crucial components stand out: the working and reference standards.
While both play a pivotal role in the pharma sector, they serve distinct purposes. This blog explains the differences between high-quality reference standards and working standards.
What is a Reference Standard?
In pharma, a reference standard is a highly purified compound used as a benchmark for analytical testing. Generally sourced from certified reference standards materials suppliers like USP (United States Pharmacopoeia) and EP (European Pharmacopoeia), these reference standards undergo strict testing and certification to ensure their accuracy and reliability.
Uses of Reference Standards
What is the Working Standard?
After reference standards come the working standard, which is primarily used for routine analysis and daily quality control testing in laboratories. A pharmaceutical reference standards supplier makes working standards in-house and compares them with standard ones to check their potency and suitability.
Uses of Working Standards
Ultimately, these standards from certified reference materials suppliers play a pivotal role in the pharmaceutical sector. Reference standards are the benchmark for accuracy and compliance while working standards provide a practical solution for quality control and daily operations.