Methodology of the formation of National standards of Good Pharmacy Practice and standard operating procedures system
DOI:
https://doi.org/10.14739/2409-2932.2019.2.171076Keywords:
Good Pharmacy Practice, standard operating procedure, national standard, guidelineAbstract
The aim of the work is the development of system of National standards of Good Pharmacy Practice (GPP) and standard operating procedures (SOPs).
Materials and methods. The research materials were legal acts of Ukraine, Guidelines on GPP, materials of professional public organizations of different countries on the issues of quality assurance of pharmacy services. Methods of logical and system-structural analysis, modeling processes were used.
Results. A comparative analysis of the definitions of the term “standard operating procedure” in the domestic legislation has been conducted. A number of advantages of SOPs in practice have been highlighted. The normative regulation of pharmaceutical activity in developed countries and post-Soviet countries has been analyzed, which allows to assert the use of SOPs to meet the requirements of the quality standards of pharmacy services. Different approaches to the definition of GPP standards and the establishment of the list of SOPs have been identified.
Taking into account international experience and national peculiarities of the implementation of good practices, the following structure of the Guidance with GPP in Ukraine was proposed. It consists of: Introduction, Glossary, 8 process guides (Quality management; Receiving, storing and disposing of medicines and medical products; Preparation of medicines in the pharmacy; Prescription and non-prescription medicines delivery and medical products; Providing effective pharmacotherapy; Professional development of pharmacy staff; Improving the effectiveness of the public health system; Self-Inspection); Sources of information.
This structure of the proposed Guidance with GPP is focused on the content and functional-role approach to the development of national standards of pharmacy practices. They establish rules and give recommendations for the development of the list of SOPs for a particular pharmacy.
Conclusions. There is no definition of the term SOP in normative legal acts which directly regulate the activity of pharmacy establishments in Ukraine. Different approaches to the formation of the list of SOPs in the countries of Europe and the post-Soviet area were found. The structure of the GPP Guidance was proposed based on a functional-role approach to the development of national standards, which includes eight separate process guides that are specific to pharmacies activity.
References
(2011) Nalezhna aptechna praktyka: Standarty yakosti aptechnykh posluh (Spilna nastanova MFF/VOOZ z NAP) [Good Pharmacy Practice: standards for quality of pharmacy services (Joint FIP/WHO guidelines on GPP)]. Retrieved from http://zakon4.rada.gov.ua/laws/show/897_009 [in Ukrainian].
Zakonodavstvo Ukrainy [Ukrainian legislation]. Retrieved from https://zakon.rada.gov.ua. [in Ukrainian].
Podpruzhnykov, Yu. V., Nemchenko, A. S., Andriukova, L. N., et al. (2017) Sistema kachestva i nadlezhashchie praktiki v farmacii [Quality system and good practices in pharmacy]. Kyiv. [in Russian].
Zdoryk, O. A. (2015) Development of standard operating procedures and their introduction in compounding pharmacies. Visnyk farmatsii, 3. 56–59. doi: https://doi.org/10.24959/nphj.15.2042 [in Ukrainian].
Eiben, H. S. (2011) Pryntsypy funktsionuvannia systemy yakosti subiektiv farmatsevtychnoi diialnosti (Avtoref. dis…kand. faem. nauk) [Principles of the functioning of a quality system for companies in the field of pharmaceuticals] (Extended abstract of candidate’s thesis). Kyiv. [in Ukrainian].
Lebedinets, V. A., Kovalenko, S. N., & Takhtaulova, N. A. (2011) Rehlamentatsiia dokumentoobihu v systemi upravlinnia yakistiu farmatsevtychnoho pidpryiemstva [Regulation of document circulation in quality management system of the pharmaceutical enterprise]. Upravlinnia, ekonomika ta zabezpechennia yakosti v farmatsii, 5, 15–20. [in Ukrainian].
Leitlinien [Guidelines]. Retrieved from https://www.abda.de/themen/apotheke/qualitaetssicherung0/leitlinien/
Inspections Protokol Drogerien Retrieved from https://www.gef.be.ch/gef/de/index/direktion/organisation/kapa/formulare.assetref/dam/documents/GEF/KAPA/de/CL_0510_02_D_V02_Inspro_Dro_%20Mai2017.pdf
Standard Operating Procedures (SOPs). Retrieved from https://www.thepsi.ie/gns/inspection-enforcement/inspections/InspectorsAdvice/ SOPs.aspx.
(2007) Poryadok razrabotki rabochikh instrukcij i standartnykh operacionnykh procedur dlya aptechnykh organizacij Respubliki Belarus' [The order of development of work instructions and standard operating procedures for pharmaceutical organizations of the Republic of Belarus]. Retrieved from http://rceth.by/Documents/3mz6in20070918N050-0807.pdf [in Russian].
(2006) Postanovlenie Ministerstva zdravoohranenija Respubliki Belarus' «Ob utverzhdenii nadlezhashhih farmacevticheskih praktik» ot 27.12.2006 №120 [Resolution of the Ministry of Health of the Republic of Belarus «On approval of Good Pharmacy Practice» from December 27, 2006, №120]. Retrieved from www.pharmacia.by/downloads/05.rtf [in Russian].
(2015) Рrikaz Ministra zdravoohraneniya i social'nogo razvitiya Respubliki Kazahstan «Ob utverjdenii nadlejaschih farmatsevticheskih praktik Prikaz Ministra zdravoohraneniya i sotsialnogo razvitiya Respubliki Kazahstan» ot 27.05.2015 №392 [Order of the Minister of Health and Social Development of the Republic of Kazakhstan «On approval of Good Pharmaceutical Practices» from May 27, 2015 №392]. Retrieved from https://tengrinews.kz/zakon/pravitelstvo_respubliki_kazahstan_premer_ministr_rk/zdravoohranenie/id-V1500011506. [in Russian].
(2011) Postanovlenie pravitelstva Kyirgyizskoy Respubliki «Ob utverjdenii Tehnicheskogo reglamenta «O bezopasnosti lekarstvennyih sredstv dlya meditsinskogo primeneniya» ot 06.04.2011 №137 [Resolution of the Government of the Kyrgyz Republic «On approval of the Technical Regulations “About safety of medicines for medical use”» from April 06, 2011 №137]. Retrieved from http://cbd.minjust.gov.kg/act/view/ru-ru/92533. [in Russian].
(2016) Gosudarstvennyy standart Uzbekistana. Nadlezhaschaya aptechnaya praktika [State standard of Uzbekistan. Good Pharmacy Practice]. Retrieved from http://www.uzpharm-control.uz/uploads/documents/doc-3887-09-04-2018.pdf [in Russian].
(2016) Prikaz Ministerstva zdravoohraneniya Rossijskoj Federacii «Ob utverjdenii Pravil nadlejaschey aptechnoy praktiki lekarstvennyih preparatov dlya meditsinskogo primeneniya» ot 31.08.2016 №647n [Order of the Ministry of Health of the Russian Federation «On approval of the Rules for good pharmacy practice of medicines for medical use» from August 31, 2016 №647n]. Retrieved from http://pravo.gov.ru/proxy/ips/?docbody=&nd =102421759. [in Russian].
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