The Req-Less Podcast
We spoke with a clinical pharmacologist, prinicpal investigator, and a bioanalytical sciences head about the negative impacts they have experienced within clinical trials. We discussed how sample issues impact data quality for clinical pharmacological evaluation, the impact of sample queries adding to site burden, the importance of proper sample tracking to enable bioanalytical labs to run assays in a timely fashion, and ethical implications and undue patient burden of lost samples.
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