Documentation of Pharmaceutical Development. Part 2. Quality System Documents
| Autor: | I. E. Smekhova, L. V. Shigarova, I. A. Narkevich, E. V. Flisyuk, V. D. Meteleva |
|---|---|
| Rok vydání: | 2021 |
| Předmět: |
Process management
business.industry Computer science media_common.quotation_subject Pharmaceutical Science 030204 cardiovascular system & hematology documentation pharmaceutical development 03 medical and health sciences 0302 clinical medicine Quality management system Documentation Drug Discovery New product development Change management (engineering) 030211 gastroenterology & hepatology Quality (business) Product (category theory) pharmaceutical quality system HD9665-9675 business Quality assurance Pharmaceutical industry Enterprise planning system media_common |
| Zdroj: | Разработка и регистрация лекарственных средств, Vol 10, Iss 2, Pp 147-153 (2021) |
| ISSN: | 2658-5049 2305-2066 |
| DOI: | 10.33380/2305-2066-2021-10-2-147-153 |
| Popis: | Introduction. In the process of pharmaceutical development of a medicinal product, it is necessary to substantiate the composition of the medicinal product; develop a technology for a finished dosage form (including a primary packaging system); create documentation for various stages of product development; validate analytical methods and technological processes. Information obtained in the course of experimental research and development of a medicinal product is included in the registration dossier. Documenting a pharmaceutical development allows you to systematize knowledge about monitoring technological processes, product quality indicators, and present the integrity of the data obtained.Aim. Creation of documentation for pharmaceutical development within the pharmaceutical quality system of the enterprise.Materials and methods. In the course of the research, the following methods were used: content analysis; system analysis; systems approach.Results and discussion. On the pharmaceutical development of two-component suppositories within the FGC, based on the knowledge gained about the process and the product and taking into account the risk analysis, we have created documents that were adapted to the enterprise's document flow to optimize the documentation process at the subsequent stages of the drug's life cycle. For optimal documentation of the first stage of drug development, a list of documents is proposed, including: Report on the pharmaceutical development of two-component suppositories; specifications for raw materials and materials, intermediate products, finished products; standard operating procedures during the pharmaceutical development phase; Guidelines for monitoring processes and product quality; Instructions for corrective and preventive actions (CAPA), change management, management review; report on the analysis of the effectiveness of the quality assurance system in the pharmaceutical development of two-component suppositories. The proposed set of documents makes it possible to form a single base of knowledge and results obtained at this stage, to systematize and structure them.Conclusion. In the course of the pharmaceutical development of two-component suppositories, knowledge has been generated about the process of creating a product of proper quality. A set of documents has been developed, consisting of reports, specifications, standard operating procedures, instructions, for an enterprise planning to produce two-component suppositories. Pharmaceutical development documentation is adapted to the enterprise document flow to optimize the documenting process at the subsequent stages of the drug product life cycle. |
| Databáze: | OpenAIRE |
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