Changes to the EAEU Guideline on Good Pharmacovigilance Practices

By Decision No. 81 of 19.06.2022, the Council of the Eurasian Economic Commission amended the Guideline on Good Pharmacovigilance Practices of the Eurasian Economic Union (EAEU GVP Guideline), the core regulatory document on pharmacovigilance requirements for the EAEU Member States. The amendment in...

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Main Author: B. K. Romanov
Format: Article
Language:Russian
Published: Ministry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products» 2023-03-01
Series:Безопасность и риск фармакотерапии
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Online Access:https://www.risksafety.ru/jour/article/view/336
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author B. K. Romanov
author_facet B. K. Romanov
author_sort B. K. Romanov
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description By Decision No. 81 of 19.06.2022, the Council of the Eurasian Economic Commission amended the Guideline on Good Pharmacovigilance Practices of the Eurasian Economic Union (EAEU GVP Guideline), the core regulatory document on pharmacovigilance requirements for the EAEU Member States. The amendment involved all critical pharmacovigilance processes, and its consequences are yet to be assessed.The aim of the study was to analyse the changes to the EAEU GVP Guideline effective since 06.12.2022.The author summarised information on the changes made to the EAEU GVP Guideline by Decision No. 81 of the Council of the Eurasian Economic Commission of 19.06.2022 “On Amendments to the Rules of Good Pharmacovigilance Practice of the Eurasian Economic Union”. He described the differences between the old and the new versions of the EAEU GVP Guideline. Having critically reviewed the updated regulatory document, the author commented on its positive and negative aspects. The review created a starting point for further analysis of the changes to the EAEU GVP Guideline. At the time of writing, there were no other published works assessing the significance of most of the changes for the pharmaceutical industry and designated pharmacovigilance organi­sations in the EAEU Member States. The author assessed their significance through the prism of the recent years’ events in Russia and the world, including the COVID-19 pandemic. In connection with the amended guideline coming into force in 2022, the author suggested a transitional standstill period for both the pharmaceutical industry and designated pharmacovigilance organisations. He offered further improvements for the guideline. The article may be of practical interest to pharmacovigilance specialists, heads of pharmaceutical organisations, and employees of regulatory authorities.
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spelling doaj-art-6332103c831140b58981036a69fcd34b2025-08-20T03:43:01ZrusMinistry of Health of the Russian Federation, Federal State Budgetary Institution «Scientific Centre for Expert Evaluation of Medicinal Products»Безопасность и риск фармакотерапии2312-78212619-11642023-03-01111142110.30895/2312-7821-2023-11-1-336279Changes to the EAEU Guideline on Good Pharmacovigilance PracticesB. K. Romanov0N.I. Pirogov Russian National Research Medical UniversityBy Decision No. 81 of 19.06.2022, the Council of the Eurasian Economic Commission amended the Guideline on Good Pharmacovigilance Practices of the Eurasian Economic Union (EAEU GVP Guideline), the core regulatory document on pharmacovigilance requirements for the EAEU Member States. The amendment involved all critical pharmacovigilance processes, and its consequences are yet to be assessed.The aim of the study was to analyse the changes to the EAEU GVP Guideline effective since 06.12.2022.The author summarised information on the changes made to the EAEU GVP Guideline by Decision No. 81 of the Council of the Eurasian Economic Commission of 19.06.2022 “On Amendments to the Rules of Good Pharmacovigilance Practice of the Eurasian Economic Union”. He described the differences between the old and the new versions of the EAEU GVP Guideline. Having critically reviewed the updated regulatory document, the author commented on its positive and negative aspects. The review created a starting point for further analysis of the changes to the EAEU GVP Guideline. At the time of writing, there were no other published works assessing the significance of most of the changes for the pharmaceutical industry and designated pharmacovigilance organi­sations in the EAEU Member States. The author assessed their significance through the prism of the recent years’ events in Russia and the world, including the COVID-19 pandemic. In connection with the amended guideline coming into force in 2022, the author suggested a transitional standstill period for both the pharmaceutical industry and designated pharmacovigilance organisations. He offered further improvements for the guideline. The article may be of practical interest to pharmacovigilance specialists, heads of pharmaceutical organisations, and employees of regulatory authorities.https://www.risksafety.ru/jour/article/view/336eurasian economic uniondrug safetypharmacovigilanceguideline on good pharmacovigilance practicegvpchanges to gvp
spellingShingle B. K. Romanov
Changes to the EAEU Guideline on Good Pharmacovigilance Practices
Безопасность и риск фармакотерапии
eurasian economic union
drug safety
pharmacovigilance
guideline on good pharmacovigilance practice
gvp
changes to gvp
title Changes to the EAEU Guideline on Good Pharmacovigilance Practices
title_full Changes to the EAEU Guideline on Good Pharmacovigilance Practices
title_fullStr Changes to the EAEU Guideline on Good Pharmacovigilance Practices
title_full_unstemmed Changes to the EAEU Guideline on Good Pharmacovigilance Practices
title_short Changes to the EAEU Guideline on Good Pharmacovigilance Practices
title_sort changes to the eaeu guideline on good pharmacovigilance practices
topic eurasian economic union
drug safety
pharmacovigilance
guideline on good pharmacovigilance practice
gvp
changes to gvp
url https://www.risksafety.ru/jour/article/view/336
work_keys_str_mv AT bkromanov changestotheeaeuguidelineongoodpharmacovigilancepractices