Literature DB >> 17716847

Harmonization of strategies for the validation of quantitative analytical procedures. A SFSTP proposal--part III.

Ph Hubert1, J-J Nguyen-Huu2, B Boulanger3, E Chapuzet4, N Cohen5, P-A Compagnon6, W Dewé7, M Feinberg8, M Laurentie9, N Mercier4, G Muzard10, L Valat11, E Rozet12.   

Abstract

In the first two documents [Ph. Hubert, J.J. Nguyen-Huu, B. Boulanger, E. Chapuzet, P. Chiap, N. Cohen, P.A. Compagnon, W. Dewé, M. Feinberg, M. Lallier, M. Laurentie, N. Mercier, G. Muzard, C. Nivet, L. Valat, J. Pharm. Biomed. Anal. 36 (2004) 579-586; Ph. Hubert, J.J. Nguyen-Huu, B. Boulanger, E. Chapuzet, P. Chiap, N. Cohen, P.A. Compagnon, W. Dewé, M. Feinberg, M. Lallier, M. Laurentie, N. Mercier, G. Muzard, C. Nivet, L. Valat, E. Rozet, J. Pharm. Biomed. Anal., in press], a recent SFSTP Commission on the validation of analytical procedure has introduced a harmonized approach for the validation of analytical procedures. In order to complete this guide, the statistical methodology allowing to correctly conclude about the validity of a procedure is proposed in this third part of the guide. Indeed all the steps to obtain the decision tool namely the accuracy profile are described and illustrated step by step by a numerical example. This tool, based on the concept of total error (bias+standard deviation) build with a beta-expectation tolerance interval, allows to easily take the right decision and simultaneously minimizing the risk of the future use of the analytical procedure.

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Year:  2007        PMID: 17716847     DOI: 10.1016/j.jpba.2007.06.032

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  20 in total

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2.  Validation of alternative methods for the analysis of drinking water and their application to Escherichia coli.

Authors:  Abdelkader Boubetra; François Le Nestour; Corrie Allaert; Max Feinberg
Journal:  Appl Environ Microbiol       Date:  2011-03-25       Impact factor: 4.792

3.  Evaluation of the stability of vancomycin solutions at concentrations used in clinical services.

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4.  HPLC method with post-column derivatization for the analysis of endogenous histidine in human saliva validated using the total-error concept.

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Journal:  Amino Acids       Date:  2022-02-19       Impact factor: 3.520

5.  Development and Validation of an HPLC-UV Method for the Dissolution Studies of 3D-Printed Paracetamol Formulations in Milk-Containing Simulated Gastrointestinal Media.

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Journal:  Pharmaceuticals (Basel)       Date:  2022-06-16

6.  Physicochemical stability of oxycodone-ketamine solutions in polypropylene syringe and polyvinyl chloride bag for patient-controlled analgesia use.

Authors:  Mikaël Daouphars; Charles-Henri Hervouët; Pierre Bohn; Delphine Martin; Jean Rouvet; Florence Basuyau; Rémi Varin
Journal:  Eur J Hosp Pharm       Date:  2016-10-17

7.  High-Throughput NIR-Chemometric Method for Meloxicam Assay from Powder Blends for Tableting.

Authors:  Ioan Tomuta; Rares Iovanov; Andreea Loredana Vonica; Sorin E Leucuta
Journal:  Sci Pharm       Date:  2011-10-13

8.  Ultra High Performance Liquid Chromatography Method for the Determination of Two Recently FDA Approved TKIs in Human Plasma Using Diode Array Detection.

Authors:  Marwa Fouad; Maxime Helvenstein; Bertrand Blankert
Journal:  J Anal Methods Chem       Date:  2015-05-25       Impact factor: 2.193

Review 9.  Good quantification practices of flavours and fragrances by mass spectrometry.

Authors:  Frédéric Begnaud; Alain Chaintreau
Journal:  Philos Trans A Math Phys Eng Sci       Date:  2016-10-28       Impact factor: 4.226

10.  Assessment of isoflavone aglycones variability in soy food supplements using a validated HPLC-UV method.

Authors:  Alina Uifălean; Anca Farcaş; Maria Ilieş; Simona Codruţa Hegheş; Corina Ionescu; Cristina Adela Iuga
Journal:  Clujul Med       Date:  2015-07-01
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