Sammenlign metoder

	Validering af analytiske metoder	UV-Vis-spektrofotometri
Fagområde	Analytisk kemi	Analytisk kemi
Familie	Process / pipeline	Process / pipeline
Oprindelsesår	1995	1852
Ophavsperson	FDA and ICH regulatory agencies	August Beer
Type	regulatory and quality control framework	absorption measurement technique
Oprindelig kilde	Food and Drug Administration. (2015). Analytical Procedures and Methods Validation: Chemistry, Manufacturing, and Controls Documentation. FDA Guidance for Industry.	Beer, A. (1852). Bestimmung der Absorption des rothen Lichts in farbigen Flussigkeiten. Annalen der Physik und Chemie, 86(5), 78–88.
Aliasser	method validation, analytical validation, OOS investigation, protocol validation	UV-Vis spectroscopy, absorption spectroscopy, colorimetry
Relaterede	5	5
Resumé	Analytical method validation is a systematic process of establishing documented evidence that an analytical method is suitable for its intended use in measuring the identity, purity, strength, and/or content of a substance. Governed by regulatory agencies (FDA, ICH) and industry standards (USP, EP), validation ensures that analytical methods are reliable, accurate, and suitable for quality control in pharmaceutical, food, chemical, and environmental industries. Method validation is mandatory for regulatory submissions and is a cornerstone of good manufacturing practice (GMP).	UV-Vis spectrophotometry is an optical analytical technique that measures the absorption of ultraviolet and visible light (wavelengths 190–900 nm) by substances in solution. Founded on the Beer-Lambert law (developed by August Beer and Pierre Bouguer), it is one of the oldest and most widely used quantitative analytical methods. UV-Vis spectrophotometry is economical, rapid, and applicable to a vast range of organic and inorganic compounds, making it indispensable in pharmaceutical, clinical, environmental, and research laboratories.