Background
Heart Study has been operating for more than 40Â years, and throughout that time it has found a number of risk variables that interact negatively to have an overall negative effect on cardiovascular disease (CVD) with an estimated 17.9 million deaths per year, CVD is the world's leading cause of death.
Main body
In the current study, we present spectrophotometric, chromatographic analysis and bioanalysis methods for qualitative and quantitative evaluation of 15 drugs, including small and large molecules, that the U.S. FDA approved between 2015 and June 2020 to treat CVD’s and in the current review work, they were presented.
Short conclusion
The review's conclusion is that spectroscopic, chromatographic and bioanalysis methods play important role in quality control and standardization of recently approved drugs from 2015 to 2020 for treating CVD’s in its bulk, pharmaceutical dosage form, synthetic mixture or human/rat plasma.