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Journal Abstract Search

124 related items for PubMed ID: 913539

  • 21. Guest editors' note: special issue on recent developments in statistical approaches for chemistry and manufacturing control (CMC) and quality-by-design(QbD).
    Tsong Y, Yang H.
    J Biopharm Stat; 2015; 25(2):233. PubMed ID: 25437635
    [No Abstract] [Full Text] [Related]

  • 22. [Role of the Pharmacopoeia Committee of the Ministry of Public Health of the USSR in improving drug preparation quality].
    Oboĭmakova OM.
    Farm Zh; 1977; 32(4):28-31. PubMed ID: 913542
    [No Abstract] [Full Text] [Related]

  • 23.
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  • 25. Roadmap for implementation of quality by design (QbD) for biotechnology products.
    Rathore AS.
    Trends Biotechnol; 2009 Sep; 27(9):546-53. PubMed ID: 19647883
    [Abstract] [Full Text] [Related]

  • 26. [Role of analytical control laboratories in improving the quality of drug production].
    Kulesheva MS.
    Farm Zh; 1977 Sep; 32(4):35-9. PubMed ID: 913545
    [No Abstract] [Full Text] [Related]

  • 27.
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  • 29. [Measurement and quality control of drug forms. 24. Linear optimization of pharmaceutico-technological production of mixtures of substances].
    Zácek H.
    Pharm Acta Helv; 1983 Sep; 58(12):325-31. PubMed ID: 6657710
    [No Abstract] [Full Text] [Related]

  • 30. WHO Expert Committee on Specifications for Pharmaceutical Preparations.
    World Health Organization.
    World Health Organ Tech Rep Ser; 2011 Sep; (961):1-428, back cover. PubMed ID: 21699061
    [Abstract] [Full Text] [Related]

  • 31. [Tasks of the pharmacy network and service in improving the control of drug quality in light of the decisions of the 25th Congress of the CPSU].
    Uzdennikov OM.
    Farm Zh; 1977 Sep; 32(4):10-3. PubMed ID: 913537
    [No Abstract] [Full Text] [Related]

  • 32. July-August 2020 Issue.
    Levy R.
    PDA J Pharm Sci Technol; 2020 Sep; 74(4):367. PubMed ID: 32737241
    [No Abstract] [Full Text] [Related]

  • 33. [Tasks in the field of improving the quality of synthetic chemico-pharmaceutical preparations].
    Zasosov VA.
    Med Prom SSSR; 1966 Oct; 20(10):24-8. PubMed ID: 6000055
    [No Abstract] [Full Text] [Related]

  • 34. [Mathematical modeling and optimizing pharmaceutical, technological quality control of drugs].
    Leuenberger H, Guitard P, Sucker H.
    Pharm Unserer Zeit; 1976 May; 5(3):65-76. PubMed ID: 959248
    [No Abstract] [Full Text] [Related]

  • 35. [Testing and quality control of drug preparations. IX. Methods of granulometric analysis of drug preparations].
    Zácek H.
    Cesk Farm; 1973 Apr; 22(3):126-9. PubMed ID: 4701739
    [No Abstract] [Full Text] [Related]

  • 36. Estimation of the probability of passing the USP dissolution test.
    Wang H.
    J Biopharm Stat; 2007 Apr; 17(3):407-13. PubMed ID: 17479390
    [Abstract] [Full Text] [Related]

  • 37. [Work productivity--toward new higher levels].
    Iurskova ZF.
    Med Tekh; 1983 Apr; (5):3-7. PubMed ID: 6645849
    [No Abstract] [Full Text] [Related]

  • 38. [Problems of control of polymers used in drug technology].
    Krówczyński L.
    Polim Med; 1984 Apr; 14(1-4):5-12. PubMed ID: 6533635
    [Abstract] [Full Text] [Related]

  • 39. Quality assurance during the production process.
    Tucker JD.
    Med Serv J Can; 1967 Mar; 23(3):262-9. PubMed ID: 6056371
    [No Abstract] [Full Text] [Related]

  • 40. Application of the near-infrared spectroscopy in the pharmaceutical technology.
    Jamrógiewicz M.
    J Pharm Biomed Anal; 2012 Jul; 66():1-10. PubMed ID: 22469433
    [Abstract] [Full Text] [Related]

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