000 01461 a2200421 4500
005 20250516005546.0
264 0 _c20110520
008 201105s 0 0 eng d
022 _a1873-264X
024 7 _a10.1016/j.jpba.2010.09.024
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aOldenhof, M T
245 0 0 _aConsistency of FMEA used in the validation of analytical procedures.
_h[electronic resource]
260 _bJournal of pharmaceutical and biomedical analysis
_cFeb 2011
300 _a592-5 p.
_bdigital
500 _aPublication Type: Journal Article
650 0 4 _aChromatography, High Pressure Liquid
650 0 4 _aClinical Laboratory Techniques
650 0 4 _aEquipment Failure Analysis
650 0 4 _aMass Spectrometry
650 0 4 _aPharmaceutical Preparations
_xanalysis
650 0 4 _aProbability
650 0 4 _aQuality Control
650 0 4 _aReproducibility of Results
650 0 4 _aRisk Assessment
650 0 4 _aRisk Management
650 0 4 _aSensitivity and Specificity
650 0 4 _aValidation Studies as Topic
700 1 _avan Leeuwen, J F
700 1 _aNauta, M J
700 1 _ade Kaste, D
700 1 _aOdekerken-Rombouts, Y M C F
700 1 _aVredenbregt, M J
700 1 _aWeda, M
700 1 _aBarends, D M
773 0 _tJournal of pharmaceutical and biomedical analysis
_gvol. 54
_gno. 3
_gp. 592-5
856 4 0 _uhttps://doi.org/10.1016/j.jpba.2010.09.024
_zAvailable from publisher's website
999 _c20271618
_d20271618