One of the most critical factors in developing and marketing pharmaceutical drug products and dietary supplements today is ensuring that the analytical methodology used for analysis will produce high quality, valid data, which is used to make sound business and regulatory decisions. Global regulatory agencies like the FDA, USP and EP, together with standard organizations such as ASTM, ANSI and IEC, have all recognized the importance of this to the drug development process and have separately expanded method validation requirements in recent years. In this application note, we will discuss the how Raman spectroscopy, in particular the NanoRam handheld Raman spectrometer enables you to comply with all of these regulations and reduce overhead all at the same time.
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