My company has recently acquired an FTIR for incoming raw material identification. I am looking to get reference standards for some of our ingredients, but I am running in to the argument of USP standards verses reagent or ACS standards. We have about 500 different incoming raw materials so USP reference standards will be costly. Is it necessary from an FDA standpoint to obtain USP standards for raw materials or would reagent grade or ACS grade work as well? Would FTIR spectra be noticeably different using an USP verses a ACS grade? We are not using HPLC or GC, this is to collect spectra for an in house library, also only using qualitatively. Also we fall into the dietary supplement category, so we are not making pharmaceuticals.
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