Good Pharmacovigilance Practice in the United States and the European Union

The article presents the results of a comparative analysis of Goodpharmacovigilance practices (GVP), developed by experts of the regulatory bodiesof the European Union (EU) and the United States. It is shown that the EU GVP cover almost all possible aspects of pharmacovigilance. It is noted that the...

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Main Authors: V. A. Merkulov, N. D. Bunyatyan, A. P. Pereverzev
Format: Article
Language:Russian
Published: Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products» 2022-06-01
Series:Безопасность и риск фармакотерапии
Subjects:
Online Access:https://www.risksafety.ru/jour/article/view/318
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author V. A. Merkulov
N. D. Bunyatyan
A. P. Pereverzev
author_facet V. A. Merkulov
N. D. Bunyatyan
A. P. Pereverzev
author_sort V. A. Merkulov
collection DOAJ
description The article presents the results of a comparative analysis of Goodpharmacovigilance practices (GVP), developed by experts of the regulatory bodiesof the European Union (EU) and the United States. It is shown that the EU GVP cover almost all possible aspects of pharmacovigilance. It is noted that the disadvantages of EU GVP are difficulties in the correct understanding and interpretation of certain definitions and processes, as well as the complexity of the implementation in practice of a number of provisions, mainly related to the organization of the quality management system, including audit and inspection. As the basis for development of the Russian Rules GVP is recommended to use the GVP EU
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institution Kabale University
issn 2312-7821
2619-1164
language Russian
publishDate 2022-06-01
publisher Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products»
record_format Article
series Безопасность и риск фармакотерапии
spelling doaj-art-2e8d10becbd14d1ab34f58252937bf9f2025-08-20T03:56:38ZrusMinistry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products»Безопасность и риск фармакотерапии2312-78212619-11642022-06-01042328250Good Pharmacovigilance Practice in the United States and the European UnionV. A. Merkulov0N. D. Bunyatyan1A. P. Pereverzev2Scientific Centre for Expert Evaluation of Medicinal Products Russian FederationScientific Centre for Expert Evaluation of Medicinal Products Russian FederationScientific Centre for Expert Evaluation of Medicinal Products Russian FederationThe article presents the results of a comparative analysis of Goodpharmacovigilance practices (GVP), developed by experts of the regulatory bodiesof the European Union (EU) and the United States. It is shown that the EU GVP cover almost all possible aspects of pharmacovigilance. It is noted that the disadvantages of EU GVP are difficulties in the correct understanding and interpretation of certain definitions and processes, as well as the complexity of the implementation in practice of a number of provisions, mainly related to the organization of the quality management system, including audit and inspection. As the basis for development of the Russian Rules GVP is recommended to use the GVP EUhttps://www.risksafety.ru/jour/article/view/318good pharmacovigilance practices, gvp, european union, eu, united states
spellingShingle V. A. Merkulov
N. D. Bunyatyan
A. P. Pereverzev
Good Pharmacovigilance Practice in the United States and the European Union
Безопасность и риск фармакотерапии
good pharmacovigilance practices, gvp, european union, eu, united states
title Good Pharmacovigilance Practice in the United States and the European Union
title_full Good Pharmacovigilance Practice in the United States and the European Union
title_fullStr Good Pharmacovigilance Practice in the United States and the European Union
title_full_unstemmed Good Pharmacovigilance Practice in the United States and the European Union
title_short Good Pharmacovigilance Practice in the United States and the European Union
title_sort good pharmacovigilance practice in the united states and the european union
topic good pharmacovigilance practices, gvp, european union, eu, united states
url https://www.risksafety.ru/jour/article/view/318
work_keys_str_mv AT vamerkulov goodpharmacovigilancepracticeintheunitedstatesandtheeuropeanunion
AT ndbunyatyan goodpharmacovigilancepracticeintheunitedstatesandtheeuropeanunion
AT appereverzev goodpharmacovigilancepracticeintheunitedstatesandtheeuropeanunion