The Drug Development Process from Laboratory to Clinic

An overview of the method by which pharmaceuticals are developed, from the day in a scientist's lab when they first think of a novel drug through its ultimate approval by regulators, is provided in The Drug Development Process from Laboratory to Clinic. It explains how a discovery that potentially revolutionise a therapy is turned into a drug that is both effective and safe.
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How does one construct a bioanalytical method?

Bioanalytical methods are a set of measures that are applied across a multitude of samples. To construct your bioanalytical method, you must choose the sample and then organise and execute steps to bring each step together into a finished product. After you have done this, each step can be validated by itself to ensure consistency. Once you have this information, you will be able to construct a test and work through any issues that arise while testing.
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Standard Operating Procedures for LC-MS/MS

A potent analytical method for the identification and quantification of peptides and small compounds is liquid chromatography-tandem mass spectrometry (LC-MS/MS). To ensure accuracy, precision, and repeatability in the analysis, the use of internal standards is an essential component of LC-MS/MS. To guarantee that the approach is solid and trustworthy.
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