Literature DB >> 17646076

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

Ph Hubert1, J-J Nguyen-Huu2, B Boulanger3, E Chapuzet4, P Chiap5, N Cohen6, P-A Compagnon7, W Dewé8, M Feinberg9, M Lallier10, M Laurentie11, N Mercier4, G Muzard12, C Nivet13, L Valat14, E Rozet15.   

Abstract

As reported in a previous paper, the main objective of the new commission of the Société Française des Sciences et Techniques Pharmaceutiques (SFSTP) was the harmonisation of approaches for the validation of quantitative analytical procedures. In a series of meetings, members of this Commission have first tried to review the objectives of analytical methods and the objectives of validation methods and to recommend the use of two-sided beta-expectation tolerance intervals for total error of validation samples (accuracy profile) in the acceptance/rejection of analytical method in validation phase. In the context of the harmonization, the other objectives were: (i) to propose a consensus on the norms usually recognized, while widely incorporating the ISO terminology; (ii) to recommend to validate the analytical procedure accordingly to the way it will be used in routine; (iii) to elaborate a rational, practical and statistically reliable strategy to assure the quality of the analytical results generated. This strategy has been formalised in a guide and the three latter objectives made by the Commission are summarised in the present paper which is the second part of summary report of the SFSTP commission. The SFSTP guide has been produced to help analysts to validate their analytical methods. It is the result of a consensus between professionals having expertise in analytical and/or statistical fields. The suggestions presented in this paper should therefore help the analyst to design and perform the minimum number validation experiments needed to obtain all the required information to establish and demonstrate the reliability of its analytical procedure.

Mesh:

Year:  2007        PMID: 17646076     DOI: 10.1016/j.jpba.2007.06.013

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


  18 in total

1.  Evaluation of physiological amino acids profiling by tandem mass spectrometry.

Authors:  Romain Filee; Roland Schoos; François Boemer
Journal:  JIMD Rep       Date:  2013-11-05

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.  How to minimize toxic exposure to pyridine during continuous infusion of ceftazidime in patients with cystic fibrosis?

Authors:  P Bourget; A Amin; C Dupont; M Abely; N Desmazes-Dufeu; J C Dubus; B-L Jouani; C Merlette; R Nové-Josserand; J Pages; R Panzo; F Vidal; F Voge; D Hubert
Journal:  Antimicrob Agents Chemother       Date:  2014-03-10       Impact factor: 5.191

4.  Discriminative and quantitative analysis of norepinephrine and epinephrine by surface-enhanced Raman spectroscopy with gold nanoparticle suspensions.

Authors:  Antoine Dowek; Marion Berge; Patrice Prognon; François-Xavier Legrand; Eric Larquet; Ali Tfayli; Laetitia Minh Mai Lê; Eric Caudron
Journal:  Anal Bioanal Chem       Date:  2021-10-31       Impact factor: 4.142

5.  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

6.  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

7.  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

8.  Green Analytical Methods of Antimalarial Artemether-Lumefantrine Analysis for Falsification Detection Using a Low-Cost Handled NIR Spectrometer with DD-SIMCA and Drug Quantification by HPLC.

Authors:  Moussa Yabré; Ludivine Ferey; Abdoul Karim Sakira; Camille Bonmatin; Clotilde Fauré; Touridomon Issa Somé; Karen Gaudin
Journal:  Molecules       Date:  2020-07-27       Impact factor: 4.411

9.  Determination and analysis of ustiloxins A and B by LC-ESI-MS and HPLC in false smut balls of rice.

Authors:  Tijiang Shan; Weibo Sun; Hao Liu; Shan Gao; Shiqiong Lu; Mingan Wang; Wenxian Sun; Zhiyi Chen; Shu Wang; Ligang Zhou
Journal:  Int J Mol Sci       Date:  2012-09-10       Impact factor: 6.208

10.  Development and validation of an HPLC-MS/MS method for the determination of arginine-vasopressin receptor blocker conivaptan in human plasma and rat liver microsomes: application to a metabolic stability study.

Authors:  Haitham Alrabiah; Adnan A Kadi; Mohamed W Attwa; Gamal A E Mostafa
Journal:  Chem Cent J       Date:  2018-05-02       Impact factor: 4.215

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.