{"id":4981,"date":"2016-07-21T12:00:14","date_gmt":"2016-07-21T10:00:14","guid":{"rendered":"http:\/\/www.rapharm.eu\/hr\/2016\/07\/21\/novice-na-podrocju-regulative-medicinskih-pripomockov\/"},"modified":"2016-09-02T14:41:42","modified_gmt":"2016-09-02T12:41:42","slug":"novosti-na-podrucju-regulative-medicinskih-proizvoda-sredstava","status":"publish","type":"post","link":"https:\/\/www.rapharm.eu\/hr\/novosti-na-podrucju-regulative-medicinskih-proizvoda-sredstava\/","title":{"rendered":"Novosti na podru\u010dju regulative medicinskih proizvoda\/sredstava"},"content":{"rendered":"<style type=\"text\/css\"><\/style><p>Najkasnije do kraja godine o\u010dekuju se izmjene\u00a0EU regulative medicinskih proizvoda\/srestava koje su potrebne radi:<\/p>\n<ul>\n<li>prilaga\u0111anja tehnolo\u0161kom, znanstvenemu i regulatornom razvoju<\/li>\n<li>otklanjanja nedostataka dosada\u0161njeg sustava (ja\u010danje sigurnosti medicinskih proizvoda\/sredstava i njihovog slobodnog pretoka u okviru unutra\u0161njeg trga),<\/li>\n<li>regulatorne podr\u0161ke inovacijama i konkurentnosti industrije.<\/li>\n<\/ul>\n<p>Umjesto tri direktive, od sad \u0107e podru\u010dje ure\u0111ivati dvije uredbe. Donijeti \u0107e vi\u0161e uskla\u0111enosti kod djelovanja i jasnija pravila.<\/p>\n<p>Neposredno uz usvajanje uredbi, raPHARM \u0107e organizirati detaljno obrazovanje na tu temu.\u00a0<a href=\"http:\/\/www.rapharm.eu\/hr\/kontakt\/\">Obavijestite nas o svojem interesu ve\u0107 sad<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Najkasnije do kraja godine o\u010dekuju se izmjene\u00a0EU regulative medicinskih proizvoda\/srestava koje su potrebne radi: prilaga\u0111anja tehnolo\u0161kom, znanstvenemu i regulatornom razvoju otklanjanja nedostataka dosada\u0161njeg sustava (ja\u010danje sigurnosti medicinskih proizvoda\/sredstava i njihovog slobodnog pretoka u okviru unutra\u0161njeg trga), regulatorne podr\u0161ke inovacijama i konkurentnosti industrije. Umjesto tri direktive, od sad \u0107e podru\u010dje ure\u0111ivati dvije uredbe. Donijeti \u0107e vi\u0161e&#8230;<\/p>\n","protected":false},"author":1,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[43,41],"tags":[],"class_list":["post-4981","post","type-post","status-publish","format-standard","hentry","category-aktivno-obrazovanje","category-regulatorne-vijesti"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v25.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Novosti na podru\u010dju regulative medicinskih proizvoda\/sredstava - raPHARM<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.rapharm.eu\/novice-na-podrocju-regulative-medicinskih-pripomockov\/\" \/>\n<meta property=\"og:locale\" content=\"hr_HR\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Novosti na podru\u010dju regulative medicinskih proizvoda\/sredstava - raPHARM\" \/>\n<meta property=\"og:description\" content=\"Najkasnije do kraja godine o\u010dekuju se izmjene\u00a0EU regulative medicinskih proizvoda\/srestava koje su potrebne radi: prilaga\u0111anja tehnolo\u0161kom, znanstvenemu i regulatornom razvoju otklanjanja nedostataka dosada\u0161njeg sustava (ja\u010danje sigurnosti medicinskih proizvoda\/sredstava i njihovog slobodnog pretoka u okviru unutra\u0161njeg trga), regulatorne podr\u0161ke inovacijama i konkurentnosti industrije. 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