CREATION OF AN INFORMATION SYSTEM FOR MANAGING THE ACTIVITIES OF TESTING LABORATORIES OF AN EXPERT INSTITUTION IN THE SPHERE OF MEDICINAL PRODUCTS CIRCULATION
https://doi.org/10.30895/1991-2919-2018-8-2-103-108
Abstract
This article describes the results of Laboratory Information Management System implementation in an expert institution dealing with medicines evaluation. The purpose of the study was to evaluate the feasibility of providing digital support to the laboratories of the Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products» of the Ministry of Health of the Russian Federation and to assess the functionality of the information system in terms of coverage of functional capabilities of various classes of laboratory software. The implementation of laboratory automation systems is required by the current regulations and is in line with international approaches to organisation of the quality management. The information system implementation made it possible to computerize management of drug samples, distribution of assignments among responsible employees, storage and management of documents, and reporting of test results. It created opportunities for direct integration with laboratory equipment allowing for creation of analytical protocols without manual data transfer. The implemented solution meets all requirements and standards for the functional capabilities of laboratory information systems. A similar system could be used in chemical, pharmacological, medical and biochemical laboratories, its implementation will make it possible to meet both national and international standards. These innovations are part of the concept of CALS/PLM technologies integration into institutions management programmes.
About the Author
K. А. KoshechkinRussian Federation
Konstantin A. Koshechkin - Head of the Information Technology Division. Candidate of Biological Sciences.
8/2 Petrovsky Boulevard, Moscow 127051
References
1. Federal Law of the Russian Federation, April 12, 2010, No. 61-FZ «On Circulation of Medicines» (In Russ.)
2. Merkulov VA, Sakaeva IV, Koshechkin KA, Sboev GA. The Experience in Establishing Quality Management System in Laboratories as Exemplified by Introducing Laboratory Information System. The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products 2012;(4):11–22 (In Russ.)
3. State Standard R 33044–2014. Principles of Good Laboratory Practice. Moscow: Standartinform; 2015 (In Russ.)
4. ГОСТ Р 52249–2009. Правила производства и контроля качества лекарственных средств. М.: Стандартинформ; 2009. [State Standard R 52249–2009. Rules for the Production and Quality Control of Medicinal Products. Moscow: Standartinform; 2009 (In Russ.)]
5. Order of the Government of the Russian Federation, November 8, 2013, No. 2067-r «On Approval of the List of Documents in the Field of Standardization, Compliance with the Requirements of which the Testing Laboratories (Centers) in Conducting Laboratory Research Ensures that the Specified Testing Laboratories (Centers) Comply with the Principles of Good Laboratory Practice of the Organization for Economic Cooperation and Development» (In Russ.)
6. Decree of the Government of the Russian Federation, December 17, 2013, No. 1172 «On the Recognition and Assessment of the Conformity of Testing Laboratories (Centers) to the Principles of Good Laboratory Practice, Consistent with the Principles of Good Laboratory Practice of Organizing Economic Cooperation and Development» (In Russ.)
7. Decree of the Government of the Russian Federation, December 3, 2015, No. 1314 «On Determining the Conformity of Drug Manufacturers to the Requirements of the Rules of Good Manufacturing Practice» (In Russ.)
8. Order of the Ministry of Industry and Trade of the Russian Federation, December 21, 2015, No. 4184 «On the Definition of the Federal Budgetary Institution «State Institute of Medicines and Good Practices» of the Ministry of Industry and Trade of the Russian Federation as an Authorized Institution for Inspections» (In Russ.)
9. CFR — Code of Federal Regulations Title 21. Available from: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?CFRPart=11
10. PIC/S Guidance.Good Practices for Computerised Systems in Regulated «GxP» Environments. Available from: https://www.picscheme.org/layout/document.php?id=155
11. GAMP 5: A Risk-Based Approach to Compliant GxP Computerized Systems. Available from: https://www.ispe.org/publications/guidance-documents/gamp-5
12. Solution for the Laboratory and the Whole Enterprise — STARLIMS Laboratory Information System (In Russ.) Available from: http://12news.ru/doc5453.html
13. Myers JD. Collaborative Electronic Notebooks as Electronic Records: Design Issues for the Secure Electronic Laboratory Notebook (ELN). Proc. 2003 Western MultiConf, The Society for Modeling and Simulation, 2003. P. 13–22.
14. Shah K. Elevating Laboratory Informatics to Assist Decision-Making. Pharmaceutical Technology Europe 2009; 21(5). Available from: http://www.pharmtech.com/elevating-laboratory-informatics-assist-decision-making
15. Koshechkin KA, Olefir YuV, Merkulov VA. Management of Information Support of the Life Cycle of Medicines. Concepts of Using Elements of CALS/PLM-technologies for Information Support of the Life Cycle of Medicines. Moscow: Polygraph-Plus; 2015 (In Russ.)
Review
For citations:
Koshechkin K.А. CREATION OF AN INFORMATION SYSTEM FOR MANAGING THE ACTIVITIES OF TESTING LABORATORIES OF AN EXPERT INSTITUTION IN THE SPHERE OF MEDICINAL PRODUCTS CIRCULATION. The Bulletin of the Scientific Centre for Expert Evaluation of Medicinal Products. 2018;8(2):103-108. (In Russ.) https://doi.org/10.30895/1991-2919-2018-8-2-103-108