{"id":444318,"date":"2017-08-15T14:10:18","date_gmt":"2017-08-15T14:10:18","guid":{"rendered":"http:\/\/www.moldova.org\/en\/?p=444318"},"modified":"2017-08-15T14:11:02","modified_gmt":"2017-08-15T14:11:02","slug":"medicines-agency-signed-first-time-collaboration-agreements-two-similar-eu-institutions","status":"publish","type":"post","link":"https:\/\/www.moldova.org\/en\/medicines-agency-signed-first-time-collaboration-agreements-two-similar-eu-institutions\/","title":{"rendered":"The Medicines Agency signed, for the first time, collaboration agreements with two similar EU institutions"},"content":{"rendered":"<span class=\"span-reading-time rt-reading-time\" style=\"display: block;\"><span class=\"rt-label rt-prefix\">Reading Time: <\/span> <span class=\"rt-time\"> 2<\/span> <span class=\"rt-label rt-postfix\">minutes<\/span><\/span><p>The Agency for Medicines and Medical Devices from the Republic of Moldova has concluded cooperation agreements with the State Agency for Drug Control in the Republic of Lithuania and the Office for the Registration of Medicines, Medical Devices and Biocides from the Republic of Poland.<\/p>\n<p>The signing of these agreements is a first for AMDM, which did not previously benefit from partnerships with drug regulatory agencies in other countries.<\/p>\n<p>The collaboration agreements were signed by the AMDM General Director Vladislav Zara, along with the Lithuanian and Polish counterparts, Gintautas Barcys and Grzegorz Cessak. The agreements were signed at the meeting of the Regulatory Authorities for Medicines and Medical Devices that participated in the Twinning project that took place in the period of August 9-12, in 2017, in Warsaw.<\/p>\n<p>&#8220;With the signing of the cooperation agreements, the legal basis for effective cooperation between the Moldovan, Lithuanian and Polish regulatory institutions was established,&#8221; Vladislav Zara said.<\/p>\n<p>According to him, AMDM will benefit from the support and experience of the European partners in order to improve the legislative framework. &#8220;The conclusion of cooperation agreements with the EU Member States is a first step in establishing official relations and strengthening the AMDM status in the European network of regulatory authorities&#8221; said Vladislav Zara.<\/p>\n<p>Collaboration agreements with Lithuania and Poland will enable AMDM to strengthen its oversight activity on the pharmaceutical market in the Republic of Moldova and support the effectiveness of the health system belonging to the European standards.<\/p>\n<p>Topics related to the monitoring of the presence of medicinal products on the pharmaceutical markets in Lithuania, Poland and the Republic of Moldova were also discussed, as well as the recording and reporting of clinical and pharmacovigilance studies in the European system, EudraVigilance &#8211; the drug safety monitoring system.<\/p>\n<p>Another important topic was the Warsaw authorities&#8217; participation in the European Medicines Agency (EMA) transfer competition, which oversees the safety of medicines sold in the European Union, from the UK to Poland.<\/p>\n<p><img fetchpriority=\"high\" decoding=\"async\" class=\"alignnone size-full wp-image-444320\" src=\"http:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141.jpg\" alt=\"\" width=\"750\" height=\"562\" srcset=\"https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141.jpg 750w, https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141-300x225.jpg 300w, https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141-80x60.jpg 80w, https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141-265x198.jpg 265w, https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141-696x522.jpg 696w, https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141-560x420.jpg 560w\" sizes=\"(max-width: 750px) 100vw, 750px\" \/><\/p>\n","protected":false},"excerpt":{"rendered":"<p><span class=\"span-reading-time rt-reading-time\" style=\"display: block;\"><span class=\"rt-label rt-prefix\">Reading Time: <\/span> <span class=\"rt-time\"> 2<\/span> <span class=\"rt-label rt-postfix\">minutes<\/span><\/span>The Agency for Medicines and Medical Devices from the Republic of Moldova has concluded cooperation agreements with the State Agency for Drug Control in the Republic of Lithuania and the Office for the Registration of Medicines, Medical Devices and Biocides from the Republic of Poland. The signing of these agreements is a first for AMDM, [&hellip;]<\/p>\n","protected":false},"author":23,"featured_media":444319,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[6,4],"tags":[],"class_list":["post-444318","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-important-en","category-society"],"content_social_share":"<span class=\"span-reading-time rt-reading-time\" style=\"display: block;\"><span class=\"rt-label rt-prefix\">Reading Time: <\/span> <span class=\"rt-time\"> 2<\/span> <span class=\"rt-label rt-postfix\">minutes<\/span><\/span><p>The Agency for Medicines and Medical Devices from the Republic of Moldova has concluded cooperation agreements with the State Agency for Drug Control in the Republic of Lithuania and the Office for the Registration of Medicines, Medical Devices and Biocides from the Republic of Poland.<\/p>\n<p>The signing of these agreements is a first for AMDM, which did not previously benefit from partnerships with drug regulatory agencies in other countries.<\/p>\n<p>The collaboration agreements were signed by the AMDM General Director Vladislav Zara, along with the Lithuanian and Polish counterparts, Gintautas Barcys and Grzegorz Cessak. The agreements were signed at the meeting of the Regulatory Authorities for Medicines and Medical Devices that participated in the Twinning project that took place in the period of August 9-12, in 2017, in Warsaw.<\/p>\n<p>&#8220;With the signing of the cooperation agreements, the legal basis for effective cooperation between the Moldovan, Lithuanian and Polish regulatory institutions was established,&#8221; Vladislav Zara said.<\/p>\n<p>According to him, AMDM will benefit from the support and experience of the European partners in order to improve the legislative framework. &#8220;The conclusion of cooperation agreements with the EU Member States is a first step in establishing official relations and strengthening the AMDM status in the European network of regulatory authorities&#8221; said Vladislav Zara.<\/p>\n<p>Collaboration agreements with Lithuania and Poland will enable AMDM to strengthen its oversight activity on the pharmaceutical market in the Republic of Moldova and support the effectiveness of the health system belonging to the European standards.<\/p>\n<p>Topics related to the monitoring of the presence of medicinal products on the pharmaceutical markets in Lithuania, Poland and the Republic of Moldova were also discussed, as well as the recording and reporting of clinical and pharmacovigilance studies in the European system, EudraVigilance &#8211; the drug safety monitoring system.<\/p>\n<p>Another important topic was the Warsaw authorities&#8217; participation in the European Medicines Agency (EMA) transfer competition, which oversees the safety of medicines sold in the European Union, from the UK to Poland.<\/p>\n<p><img fetchpriority=\"high\" decoding=\"async\" class=\"alignnone size-full wp-image-444320\" src=\"http:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141.jpg\" alt=\"\" width=\"750\" height=\"562\" srcset=\"https:\/\/www.moldova.org\/en\/wp-content\/uploads\/sites\/2\/2017\/08\/m-141.jpg 750w, 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