Journal of Drug Design and Medicinal Chemistry

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Validation of Soothing Compounding Mixture Technological Process Preparation

Received: 31 October 2016    Accepted: 26 November 2016    Published: 11 January 2017
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Abstract

Validation of soothing compounding mixturetechnological process preparation in accordance with the requirements of the quality system organization was done. It is preparingserially in many pharmacies of Ukraine. Obtained results indicate conformity of the finished medicine quality with the regulatory framework requirements of Ukraine in regard to the content of all mixture components.

DOI 10.11648/j.jddmc.20160206.13
Published in Journal of Drug Design and Medicinal Chemistry (Volume 2, Issue 6, December 2016)
Page(s) 74-78
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Technological Process Validation, Compounding Preparation, Soothing Mixture

References
[1] O. Baula, I. Chekman, A. Syrovaya, S. Kovalenko, N. Gorchakova, and O. Levashova, “Modern trends in the implementation of the concept of quality assurance of medicines in Ukraine“, in Pharmaceutical Journal, vol. 4, pp. 66-75, 2014.
[2] State Pharmacopoeia of Ukraine: in 3 vol., 2-nd ed., vol. 3. Kharkiv: State enterprise “Ukrainian scientific pharmacopoeial center of medicines quality”, 2014, 732 p.
[3] State Pharmacopoeia of Ukraine: in 3 vol., 2-nd ed., vol. 1. Kharkiv: State enterprise “Ukrainian scientific pharmacopoeial center of medicines quality”, 2015, 1128 p.
[4] Joint FIP/WHO guidelines on good pharmacy practice: standards for quality of pharmacy services. WHO Technical Report Series, No. 961. Geneva: World Health Organization, 2011.
[5] L. Gala,“Evolution of good pharmaceutical practice standards in the world according to the requirements of modern pharmacy”, inPharmaceutical Review, vol. 3, pp. 63-67, 2013.
[6] S. Tiyyagura, Dr. A. Purnanand, and Dr. M. Rathinavelu, “Assessment of Good Pharmacy Practice (GPP) in Pharmacies of Community Settings in India”, in IOSR Journal of Pharmacy”, vol. 4, issue 12, pp. 27-33, December 2014.
[7] Order of the Ministry of Health of Ukraine №455 “About approval of Guideline "Good Pharmacy Practice: standards of quality pharmacy services” from 30.05.2013 [Electronic version]. Access mode: http://zakon3.rada.gov.ua/laws/show/897_009.
[8] Order of the Ministry of Health of Ukraine № 812 “About the approval of production (compounding) rules and quality control of preparations in pharmacies” from 17.10.2012 in Official Bulletin of Ukraine, vol. 87, p. 166, 2012.
[9] V. Georgiyants, O. Shtrimaitis, L. Savchenko, and E. Bisaga, “Comparison of the quantitative determination methods of the 1% solution of the sodium bromide”, in Ukrainian medical almanac, vol. 15, issue 5, pp. 51-53, 2012.
[10] State Pharmacopoeia of Ukraine: in 3 vol., 2-nd ed., vol. 2. Kharkiv: State enterprise “Ukrainian scientific pharmacopoeial center of medicines quality”, 2014, 724 p.
[11] M. Kuleshova, L. Guseva, and O. Sivitskaya, “Analysis of compounding dosage forms”, Moscow: Medicine, 1989, 228 p.
Author Information
  • Department of Quality, Standardization and Certification of Medicines, Institute of Pharmacy Professionals Qualification Improvement, National University of Pharmacy, Kharkiv, Ukraine

  • Department of Pharmaceutical Chemistry, National University of Pharmacy, Kharkiv, Ukraine

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  • APA Style

    Lesia Savchenko, Victoriya Georgiyants. (2017). Validation of Soothing Compounding Mixture Technological Process Preparation. Journal of Drug Design and Medicinal Chemistry, 2(6), 74-78. https://doi.org/10.11648/j.jddmc.20160206.13

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    ACS Style

    Lesia Savchenko; Victoriya Georgiyants. Validation of Soothing Compounding Mixture Technological Process Preparation. J. Drug Des. Med. Chem. 2017, 2(6), 74-78. doi: 10.11648/j.jddmc.20160206.13

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    AMA Style

    Lesia Savchenko, Victoriya Georgiyants. Validation of Soothing Compounding Mixture Technological Process Preparation. J Drug Des Med Chem. 2017;2(6):74-78. doi: 10.11648/j.jddmc.20160206.13

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  • @article{10.11648/j.jddmc.20160206.13,
      author = {Lesia Savchenko and Victoriya Georgiyants},
      title = {Validation of Soothing Compounding Mixture Technological Process Preparation},
      journal = {Journal of Drug Design and Medicinal Chemistry},
      volume = {2},
      number = {6},
      pages = {74-78},
      doi = {10.11648/j.jddmc.20160206.13},
      url = {https://doi.org/10.11648/j.jddmc.20160206.13},
      eprint = {https://download.sciencepg.com/pdf/10.11648.j.jddmc.20160206.13},
      abstract = {Validation of soothing compounding mixturetechnological process preparation in accordance with the requirements of the quality system organization was done. It is preparingserially in many pharmacies of Ukraine. Obtained results indicate conformity of the finished medicine quality with the regulatory framework requirements of Ukraine in regard to the content of all mixture components.},
     year = {2017}
    }
    

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