The development of an algorithm for introduction of a new drug on the existing pharmaceutical production. Stage 2. Transfer of technologies
- 作者: Basevich A.1, Dzjuba A.2, Kaukhova I.1, Tretyakova A.1, Sakharov V.1
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隶属关系:
- Saint Petersburg State Chemical and Pharmaceutical University
- JSC “PharmProject”
- 期: 卷 3, 编号 1 (2021)
- 页面: 18-30
- 栏目: Pharmaceutical Sciences
- URL: https://journals.rcsi.science/PharmForm/article/view/48535
- DOI: https://doi.org/10.17816/phf48535
- ID: 48535
如何引用文章
全文:
详细
The paper presents the results of the study based on the guidelines and scientific data on the technology transfer in the circulation of drugs. The initial data for calculations, assessment and analysis of the study results were taken from the current documentation at the operating production site of the pharmaceutical manufacturer with the participation of the company officials. The data was collected from the company work papers and job descriptions following interviews with a group of unit staff involved in the technology transfer.
The summary and the analysis of the data obtained during the research on the technology transfer for the preparation of new drugs were implemented. It was used to construct Gantt charts for some critical processes. Theassessment of the criticality of individual stages of technology transfer and a control chart of the project manager, indicating the control points of this process, was presented.
Hence, the original action plan for the new drug preparation by a pharmaceutical manufacturer has been developed: risk control and assessment system for the technology transfer project activities has been determined to assess the degree of criticality of deviations, both for the individual stages and the entire technology transfer project.
According to the objectives of the study, an original action plan for the new drug preparation by the pharmaceutical manufacturer based on the collection, processing and analysis of the data on the technology transfer at the manufacturing site has been developed.
If required, the original action plan may be tested by other drug manufacturers in the pharmaceutical industry.
作者简介
Anna Basevich
Saint Petersburg State Chemical and Pharmaceutical University
编辑信件的主要联系方式.
Email: anna.basevich@pharminnotech.com
SPIN 代码: 8189-3806
D. in Pharmaceutical Sciences, Associate Professor at the Industrial Technology of Medicines Department, Saint Petersburg State Chemical and Pharmaceutical University
俄罗斯联邦, Saint PetersburgAnatoliy Dzjuba
JSC “PharmProject”
Email: anatoly.dzuba@pharminnotech.com
Ph.D. in Pharmaceutical Sciences, Head of the Development Department, JSC “PharmProject”
俄罗斯联邦, Saint PetersburgIrina Kaukhova
Saint Petersburg State Chemical and Pharmaceutical University
Email: irina.kaukhova@pharminnotech.com
SPIN 代码: 2931-5790
Scopus 作者 ID: 736701
D.Sc. in Pharmaceutical Sciences, Professor, Head of the Industrial Technology of Medicines Department, Saint Petersburg State Chemical and Pharmaceutical University
俄罗斯联邦, Saint PetersburgArina Tretyakova
Saint Petersburg State Chemical and Pharmaceutical University
Email: arina.tretjakova@pharminnotech.com
Master Student of the faculty of Industrial Medicine Technology, Department of Economics and Management, Saint Petersburg State Chemical and Pharmaceutical University
俄罗斯联邦, Saint PetersburgVitaly Sakharov
Saint Petersburg State Chemical and Pharmaceutical University
Email: vitalij.saharov@spcpu.ru
Master Student of the faculty of Industrial Medicine Technology, Department of Industrial Ecology, Saint Petersburg State Chemical and Pharmaceutical University
俄罗斯联邦, Saint Petersburg参考
- Рудько, А. К трансферу технологий… Будь готов! / А. Рудько // Новости GMP. – 2018 – № 3 (17). – С. 70–74.
- Technology Transfer (2003). Good Practice Guide. ISPE [Internet]. Available from: http://www.fptl.ru/biblioteka/transfer/ISPE_Technology-transfer_2003.pdf.
- WHO Guidelines on transfer of technology in pharmaceutical manufacturing. WHO Technical Report Series [Internet]. 2011; 961. Available from: https://www.who.int/medicines/areas/quality_safety/quality_assurance/TransferTechnologyPharmaceuticalManufacturingTRS961Annex7.pdf
- Быковский, С.Н. Фармацевтическая разработка: концепция и практические рекомендации / С.Н. Быковский, И.А. Василенко, Н.Б. Демина [и др.] // Научно-практическое руководство для фармацевтической отрасли. – Москва: Перо, 2015. – 472 с.
- ICH Q10. Pharmaceutical Quality System [Internet]. 2008. Available from: https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q10.
- Резцов, Е. Трансфер технологий в фармацевтической отрасли / Е. Резцов // Фармацевтическая отрасль. – 2010 – № 2 (19). – С. 49–52.
- ICH Q9 (2005). Quality Risk Management. ICH Harmonised Tripartite Guideline [Internet]. 2005. Available from: https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q9/Step4/Q9_Guideline.pdf
- ICH Q8 (R2). Pharmaceutical Development. ICH Harmonised Tripartite Guideline [Internet]. 2009. Available from: https://www.ich.org/fileadmin/Public_Web_Site/ICH_Products/Guidelines/Quality/Q8_R1/Step4/Q8_R2_Guideline.pdf
- Разработка лабораторных, технологических регламентов // Reatorg: сайт. –URL: https://www.reatorg.ru/complex/predproektnaya-podgotovka-eskiznyy-proekt/razrabotka-laboratornykh-tekhnologicheskikh-reglamentov/ (дата обращения: 17.04.2019).
- Алферов, П. Концепции RIM-III. Контрольные точки / П. Алферов // Русская инструментальная модель управления проектами РИМ-III: сайт. – URL: http://rim-iii.postach.io/post/kontseptsii-rim-iii-kontrolnye-tochki (дата обращения: 17.04.2019).