UV-Visible spectroscopy is a well-established analytical technique used in the pharmaceutical industry for testing in research and quality control stages of drug development. Thermo Scientific Evolution UV-Vis Spectrophotometers provide highly accurate measurements in addition to meeting all USP and EP performance characteristics and enabling 21CFR Part 11 compliance.
Specific use cases of UV-Vis in pharmaceutical development include:
For over 60 years, customers in world-renowned research, QA/QC and educational laboratories have relied on the high-performance and exceptional value provided by Thermo Scientific UV-Visible spectrophotometers.
Compare Evolution UV-Vis models and see how they meet pharmacopeia performance requirement in this free guide: Validated Systems for Pharmaceutical Environments.
For UV-Visible spectrophotometers in regulated laboratories, performance verification at installation and at set intervals thereafter is needed. National pharmacopeias with international reach define specific performance levels for various criteria in the pharmaceutical industry.
Due to its superior specifications, the Evolution 350 UV-Vis Spectrophotometer will meet the performance needs for all global pharmacopeias including Japanese Pharmacopeia (JP), European Pharmacopeia (EP), and the United States Pharmacopeia (USP).
The Evolution 200 series will also meet all requirements for EP and USP.
Access our Pharmaceutical Standards Guide for UV-Vis Instrumentation to learn more.