HPLC Analysis of Drug Samples

The pharmaceutical industry complies with strict regulatory guideUnes in order to ensure that pharmaceutical products released to patients are appropriate for administration. This means that all products will be tested before the batch can be released to the market a series of efficacy tests are completed. When these tests are completed on the raw materials and the final preparation, certificates of analysis can also be completed. 

By examining the difference in the peak heights or by carrying out calibration and determining the actual dose present in the sample, problems with the batch can be identified. 

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