Literature DB >> 3174365

Quality control in therapeutic drug monitoring.

I C Dijkhuis1.   

Abstract

Quality control of routine drug assays, like most immunoassays, should mainly be the responsibility of each individual laboratory: intra-laboratory quality control. External quality assessment should direct its efforts in particular to non-routine methods and to new assays. However, it may sometimes also be very useful to have laboratory results of routine assays studied in external programmes, since vague requests or difficult interpretations of drug concentrations need discussion outside the individual laboratory.

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Year:  1988        PMID: 3174365     DOI: 10.1007/bf01959421

Source DB:  PubMed          Journal:  Pharm Weekbl Sci        ISSN: 0167-6555


  3 in total

1.  Laboratory performance and regulatory requirements.

Authors:  M L Kenney
Journal:  Clin Chem       Date:  1987-06       Impact factor: 8.327

2.  A survey of caffeine measurements in routine samples submitted for theophylline assay.

Authors:  J F Wilson; J Williams; R W Marshall; A Richens; I C Dijkuis; A R Harteveld; H J de Jong
Journal:  Clin Chem       Date:  1985-06       Impact factor: 8.327

3.  Interlaboratory variability in determination of plasma antiepileptic drug concentrations.

Authors:  C E Pippenger; J K Penry; B G White; D D Daly; R Buddington
Journal:  Arch Neurol       Date:  1976-05
  3 in total

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