{"id":245,"date":"2023-12-29T14:17:01","date_gmt":"2023-12-29T11:17:01","guid":{"rendered":"https:\/\/qbioresearch.com\/published-article-in-the-journal-of-safety-and-risk-of-pharmacotherapy\/"},"modified":"2024-02-13T15:18:46","modified_gmt":"2024-02-13T12:18:46","slug":"published-article-in-the-journal-of-safety-and-risk-of-pharmacotherapy","status":"publish","type":"post","link":"https:\/\/qbioresearch.com\/en\/general\/published-article-in-the-journal-of-safety-and-risk-of-pharmacotherapy\/","title":{"rendered":"Published article in the Journal of Safety and Risk of Pharmacotherapy"},"content":{"rendered":"<p style=\"font-weight: 400;\">Research and development activities of the employees of SIC Eco-safety LLC, of course, are not limited only to clinical studies. The Journal of Pharmacotherapy Safety and Risk published an original article on optimizing approaches to adverse event analysis in clinical bioequivalence studies. The authors are A.B. Verveda, V.B. Vasilyuk, G.I. Syraeva and M.V. Faraponova conducted an original study based on more than 10 years of experience in conducting clinical bioequivalence studies and in-depth analysis of the literature on mathematical modeling and pharmacosafety issues.<\/p>\n<p style=\"font-weight: 400;\">The article can be accessed at <a href=\"https:\/\/www.risksafety.ru\/jour\/article\/view\/374\/993\">https:\/\/www.risksafety.ru\/jour\/article\/view\/374\/993<\/a><\/p>\n<p style=\"font-weight: 400;\"><em>To cite<\/em><\/p>\n<p style=\"font-weight: 400;\">Verveda A.B., Vasilyuk V.B., Syraeva G.I., Faraponova M.V. Optimization of approaches to the analysis of adverse events in clinical bioequivalence studies. <em>Safety and risk of pharmacotherapy<\/em>. 2023;.  <a href=\"https:\/\/doi.org\/10.30895\/2312-7821-2023-374\">https:\/\/doi.org\/10.30895\/2312-7821-2023-374<\/a><\/p>\n<p style=\"font-weight: 400;\">Verveda A.B., Vasilyuk V.B., Syraeva G.I., Faraponova M.V. Optimization of Approaches to Adverse Event Analysis in Bioequivalence Clinical Trials. <em>Safety and Risk of Pharmacotherapy<\/em>. 2023;.  <a href=\"https:\/\/doi.org\/10.30895\/2312-7821-2023-374\">https:\/\/doi.org\/10.30895\/2312-7821-2023-374<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"Optimization of approaches to adverse event analysis in clinical bioequivalence&hellip;","protected":false},"author":1,"featured_media":134,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"footnotes":""},"categories":[24,23],"tags":[21],"class_list":["post-245","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-articles","category-general","tag-publications"],"acf":[],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.2 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Published article in the Journal of Safety and Risk of Pharmacotherapy - 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