{"id":551,"date":"2019-11-24T22:23:30","date_gmt":"2019-11-24T20:23:30","guid":{"rendered":"http:\/\/cratia.com\/?post_type=countries&#038;p=551"},"modified":"2020-11-18T17:28:42","modified_gmt":"2020-11-18T15:28:42","slug":"registracziya-mediczinskih-izdelij","status":"publish","type":"countries","link":"https:\/\/cratia.com\/en\/countries\/turkmenistan\/registracziya-mediczinskih-izdelij\/","title":{"rendered":"Registration of medical devices"},"content":{"rendered":"<p><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The main legislative act that establishes the registration requirements and circulation of medical devices is the Law of Turkmenistan \u201cOn Drug Provision\u201d. Placing on the market of Turkmenistan and putting into operation of the medical devices is allowed only after state registration.<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The competent authority responsible for the registration of medical devices is the State Registration Center for Medicinal Products of the Ministry of Health and Medical Industry of Turkmenistan.<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The Applicant (\u041dolder) of the \u041carketing \u0410uthorization can be both a resident and a non-resident of Turkmenistan. The Applicant must appoint (authorized) a local representative in Turkmenistan for regulatory purposes, which can be Cratia company.\u00a0<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The registration dossier should be submitted in the national format in Russian, Turkmen and (or) English language. The dossier should be submitted in paper form, with one identical copy.\u00a0 Samples of the medical device are submitted upon request of the competent authority.\u00a0<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">Instructions for use and the package labeling are submitted and approved in Turkmen and\/or Russian, and\/or English languages.<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The procedure of state registration includes the following steps:\u00a0<\/span><\/p>\n<ol style=\"text-align: justify;\">\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Submission of an Application and dossier to the competent authority;<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Expert evaluation of documents;<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Inclusion of devices in the State Register;<\/span><\/li>\n<li style=\"font-weight: 400;\"><span style=\"font-weight: 400;\">Issue of the Marketing Authorization.<\/span><\/li>\n<\/ol>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The validity of the Marketing Authorization (state registration certificate) is 5 years.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: justify;\"><b>Changes and amendments<\/b><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">Marketing Authorization Holder must submit the Application for variations to the competent authority within 30 days from the date of approval of such changes in the MAH\u2019s or manufacturer\u2019s country, or as soon as MAH became aware of the necessity to implement such changes. The procedure of the assessment and approval of the suggested variations can take from 1 to 3 months from the date of submission of the Application and payment of the state fees.\u00a0<\/span><\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: justify;\"><b>The renewal procedure<\/b><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">Application for renewal of the registration should be submitted not later than 3 months before the expiry of the registration certificate.\u00a0<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">The duration of the renewal procedure is 3-4 months. This period does not include the time required for the Applicant to pay state fees, and to reply to comments\/questions of the state experts.\u00a0<\/span><\/p>\n<p style=\"text-align: justify;\"><span style=\"font-weight: 400;\">As a result of the renewal procedure, a Marketing Authorization (registration certificate) is issued for the next 5 years.<\/span><\/p>\n<p>&nbsp;<\/p>\n<p style=\"text-align: justify;\"><strong>Cratia provides professional services of state registration of medical devices in Turkmenistan. We have an excellent knowledge of national legislation, necessary experience and resources.<\/strong><\/p>\n<p><span style=\"font-weight: 400;\">To start cooperation or get advice, please contact us by phone: +38 068 064-78-31, +38 044 223-61-67, by e-mail: <a href=\"mailto:info@cratia.ua\">info@cratia.ua<\/a>, or visit <a href=\"\/en\/contacts\/\">our office<\/a>.\u00a0<\/span><\/p>","protected":false},"featured_media":0,"parent":121,"menu_order":3,"template":"","class_list":["post-551","countries","type-countries","status-publish","hentry"],"acf":[],"aioseo_notices":[],"_links":{"self":[{"href":"https:\/\/cratia.com\/en\/wp-json\/wp\/v2\/countries\/551","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/cratia.com\/en\/wp-json\/wp\/v2\/countries"}],"about":[{"href":"https:\/\/cratia.com\/en\/wp-json\/wp\/v2\/types\/countries"}],"up":[{"embeddable":true,"href":"https:\/\/cratia.com\/en\/wp-json\/wp\/v2\/countries\/121"}],"wp:attachment":[{"href":"https:\/\/cratia.com\/en\/wp-json\/wp\/v2\/media?parent=551"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}