补充描述:
Solid-state control of pharmaceutical samples covers identification and quantification, method development and validation, and routine QC, using techniques such as XRPD, DSC, TGA, DVS, laser PSD, FTIR, and IDR. All analyses can handle toxic samples down to 50 ng/m3, spanning sample types from pure API to final formulations (powders, suspensions, tablets, ointments, and more), with a full detailed report including relevant literature review, comparisons, and conclusions.
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