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Journal Abstract Search

189 related items for PubMed ID: 17109871

  • 1. Content uniformity and assay requirements in current regulations.
    Bánfai B, Ganzler K, Kemény S.
    J Chromatogr A; 2007 Jul 13; 1156(1-2):206-12. PubMed ID: 17109871
    [Abstract] [Full Text] [Related]

  • 2. Probability of passing dissolution acceptance criteria for an immediate release tablet.
    Dumont ML, Berry MR, Nickerson B.
    J Pharm Biomed Anal; 2007 May 09; 44(1):79-84. PubMed ID: 17379465
    [Abstract] [Full Text] [Related]

  • 3. Content uniformity acceptance limit for a validation batch--suppositories, transdermal systems, and inhalations.
    Senderak ET.
    Drug Dev Ind Pharm; 2009 Jun 09; 35(6):735-7. PubMed ID: 19514989
    [Abstract] [Full Text] [Related]

  • 4. Letter: USP content uniformity test.
    Madan PL.
    J Pharm Sci; 1976 Jan 09; 65(1):VIII. PubMed ID: 1255410
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  • 9. Parametric two-stage sequential quality assurance test of dose content uniformity.
    Tsong Y, Shen M.
    J Biopharm Stat; 2007 Jan 09; 17(1):143-57. PubMed ID: 17219760
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  • 10. Discriminatory power of the different requirements for uniformity of dosage units in the European pharmacopoeia.
    Limberg J, Savsek M.
    Pharmeur Sci Notes; 2006 Dec 09; 2006(2):45-8. PubMed ID: 17691214
    [Abstract] [Full Text] [Related]

  • 11. Applications of NIR in early stage formulation development. Part I. Semi-quantitative blend uniformity and content uniformity analyses by reflectance NIR without calibration models.
    Li W, Bashai-Woldu A, Ballard J, Johnson M, Agresta M, Rasmussen H, Hu S, Cunningham J, Winstead D.
    Int J Pharm; 2007 Aug 01; 340(1-2):97-103. PubMed ID: 17467204
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  • 12. Results of a market surveillance study in The Netherlands on break-mark tablets.
    Barends DM, Groot DW, van der Steen JC, de Kaste D, Frijlink HW.
    Pharmeur Sci Notes; 2006 Dec 01; 2006(2):1-7. PubMed ID: 17691208
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  • 13. Sample sizes for batch acceptance from single- and multistage designs using two-sided normal tolerance intervals with specified content.
    Hauck WW, Shaikh R.
    J Biopharm Stat; 2001 Nov 01; 11(4):335-46. PubMed ID: 12018783
    [Abstract] [Full Text] [Related]

  • 14. Application of content uniformity test to tablet preparations.
    Kovács I, Hadady KK, Darbai MJ.
    Pharmazie; 1980 Nov 01; 35(10):609-12. PubMed ID: 6779284
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  • 15. Design and international harmonization of pharmacopoeial standards.
    Calam DH.
    J Pharm Biomed Anal; 1995 Dec 01; 14(1-2):1-5. PubMed ID: 8833960
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  • 16. [Exceptional Application of Content Uniformity Test and Weight Variation Test in the Japanese Pharmacopoeia 13 revision and usage of these tests for in-process tests].
    Katori N, Aoyagi N, Kojima S.
    Kokuritsu Iyakuhin Shokuhin Eisei Kenkyusho Hokoku; 1997 Dec 01; (115):204-5. PubMed ID: 9641846
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  • 19. Testing for uniformity: sampling plans in pharmacopeias for weight, volume, and content uniformity.
    Pietra V, Setnikar I.
    J Pharm Sci; 1970 Apr 01; 59(4):530-5. PubMed ID: 5440682
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  • 20. The USP content uniformity test. Analysis and proposals.
    Setnikar I.
    Pharm Acta Helv; 1974 Apr 01; 49(9-10):302-8. PubMed ID: 4462139
    [No Abstract] [Full Text] [Related]

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