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Modern Approaches to the Development of Standard Samples of Drugs

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Pharmaceutical Chemistry Journal Aims and scope

This review addresses the history of the creation of standard samples (SS) around the world and in Russia, along with studies of the current condition of the state system for standardization of medicinal products (MP) based on the use of SS. Standardization in the area of drugs is directed to guaranteeing the quality of the items standardized, which includes products (raw materials, other materials, ready MP, etc.), services, and processes. The continuing development of manufacturing technologies and the discovery of novel MP increases the need for standard samples, as drug quality control involves the use of complex, highly effective, specific, and precise physicochemical and biological analysis methods.

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Authors and Affiliations

  1. I. M. Sechenov First Moscow State Medical University (Sechenov University), Moscow, Russia

    O. Yu. Shchepochkina, V. I. Gegechkori, V. I. Prokof’eva & D. A. Chepilo

  2. State Institute for Drugs and Good Practice, Moscow, Russia

    A. A. Levko, N. N. Chadova & V. N. Shestakov

  3. Russian University of the Friendship of the Peoples, Moscow, Russia

    V. I. Gegechkori

Authors
  1. O. Yu. Shchepochkina
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  2. V. I. Gegechkori
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  3. V. I. Prokof’eva
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  4. D. A. Chepilo
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  5. A. A. Levko
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  6. N. N. Chadova
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  7. V. N. Shestakov
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Corresponding author

Correspondence to V. I. Gegechkori.

Additional information

Translated from Khimiko-Farmatsevticheskii Zhurnal, Vol. 54, No. 7, pp. 10 – 10, July, 2020.

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Shchepochkina, O.Y., Gegechkori, V.I., Prokof’eva, V.I. et al. Modern Approaches to the Development of Standard Samples of Drugs. Pharm Chem J 54, 761–765 (2020). https://doi.org/10.1007/s11094-020-02267-y

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  • DOI: https://doi.org/10.1007/s11094-020-02267-y

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