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on Validation of Analytical Procedures : Definitions and Terminology , Vol. 60 , US FDA Federal Register , 1995 . [18]. International Conference on Harmonization (ICH), Q

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selective, fast, sensitive and simple [ 3–12 ]. In order for the method to be used in quality control, its validation must be performed. If the purpose of the method is determination of impurities in finished product, following validation parameters should

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Acta Chromatographica
Authors:
A. A. Rathi
,
D. L. Dhamecha
,
M. H. G. Dehghan
,
M. Saifee
,
P. S. Wakte
,
S. D. Shelke
, and
S. H. Dongre

Pharm. Tech. 24 1 – 14 . [11]. ICH , Guidance on Analytical Method Validation , in: Proceedings of the International Convention on Quality for the Pharmaceutical

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. [20]. Guidance for Industry — Q2B Validation of Analytical Procedures: Methodology ; http://www.fda.gov/cder/guidance/index.htm .

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Guideline , Validation of Analytical Procedures: Text and Methodology Q2 (R1), Geneva, 2005, pp. 27 . [12]. R.S. Kujur V

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]. International Conference on Harmonization on Technical Requirements for Registration of Pharmaceuticals for Human Use, Validation of Analytical Procedures : Text and Methodology Q2 (R1), Geneva, 2005 . [17

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developed and validated in various countries and ethnic groups to identify patients at high risk of diabetes, but only few for prediabetes, and most have been designed for Caucasians in developed countries, and there are only a few scoring systems for Asian

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Acta Chromatographica
Authors:
Muhammad Fawad Rasool
,
Umbreen Fatima Qureshi
,
Nazar Muhammad Ranjha
,
Imran Imran
,
Mouqadus Un Nisa
, and
Abdul Majeed

liquid chromatography (RP-HPLC) is the mostly used because of high sensitivity and selectivity and economical [ 19–21 ]. This method was very economical and reliable for the determination and validation of drug in rabbit plasma and pharmaceutical dosage

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1996 Anal. Chem. 68 3520 – 3523 . [21]. ICH Q2B, Harmonized tripartite guideline, validation of analytical procedures

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