Pharmaceutical Analysis using UV-Vis: Compliance with Supplement I to the Japanese Pharmacopoeia 18th Ed., Section 2.24
Pharmaceutical Analysis using UV-Vis: Compliance with Supplement I to the Japanese Pharmacopoeia 18th Ed., Section 2.24
6 PagesWhite Paper Pharmaceutical Analysis using UV-Vis: Compliance with Supplement I to the Japanese Pharmacopoeia 18th Ed., Section 2.24 Meeting the requirements of the global pharmacopeias with the Cary 3500 UV-Vis Introduction UV-Vis spectroscopy is a widely used analytical technique in quality assurance/ quality control (QA/QC) and pharmaceutical research. It is critical that any laboratory in such environments set up appropriate controls for laboratory access and ensure that Good Manufacturing Practice (GMP) documentation, including system suitability tests (SSTs) and standard operating procedures (SOPs) are available and followed. The Japanese Pharmacopeia (JP) guidelines describe how to verify that the analytical performance of UV-Vis spectrophotometers is suitable for the i
