{"id":4876,"date":"2023-10-26T13:49:12","date_gmt":"2023-10-26T11:49:12","guid":{"rendered":"https:\/\/bemvo.be\/?page_id=4876"},"modified":"2024-07-09T18:17:28","modified_gmt":"2024-07-09T16:17:28","slug":"european-regulation-nl","status":"publish","type":"page","link":"https:\/\/bemvo.be\/index.php\/kennisdatabank\/european-regulation-nl\/","title":{"rendered":"Europese regelgeving"},"content":{"rendered":"\t\t
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\n\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t\"EUROPEAN\t\t\t\t\t\t\t\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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VEILIGHEIDSKENMERKEN VOOR GENEESMIDDELEN VOOR MENSELIJK GEBRUIK <\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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De Europese Commissie heeft een aantal specifieke antwoorden opgesteld om de implementatie van de Gedelegeerde Verordening te vergemakkelijken in een vraag en antwoord document.<\/a><\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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KENNISDATABANK EMVO<\/h2>\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t
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EMVO heeft een specifieke FAQ LIJST<\/a> opgesteld voor de houders van een vergunning voor het in de handel brengen, waarin de belangrijkste aspecten van hun verbinding met de Europese Hub worden uitgelegd.<\/p>\t\t\t\t\t\t\t\t<\/div>\n\t\t\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/div>\n\t\t\t\t\t<\/div>\n\t\t<\/section>\n\t\t\t\t

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VEILIGHEIDSKENMERKEN VOOR GENEESMIDDELEN VOOR MENSELIJK GEBRUIK De Europese Commissie heeft een aantal specifieke antwoorden opgesteld om de implementatie van de Gedelegeerde Verordening te vergemakkelijken in een vraag en antwoord document. KENNISDATABANK EMVO EMVO heeft een specifieke FAQ LIJST opgesteld voor de houders van een vergunning voor het in de handel brengen, waarin de belangrijkste aspecten […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":2613,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-4876","page","type-page","status-publish","hentry"],"yoast_head":"\nEuropese regelgeving - Bemvo<\/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:\/\/bemvo.be\/index.php\/kennisdatabank\/european-regulation-nl\/\" \/>\n<meta property=\"og:locale\" content=\"nl_NL\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Europese regelgeving - Bemvo\" \/>\n<meta property=\"og:description\" content=\"VEILIGHEIDSKENMERKEN VOOR GENEESMIDDELEN VOOR MENSELIJK GEBRUIK De Europese Commissie heeft een aantal specifieke antwoorden opgesteld om de implementatie van de Gedelegeerde Verordening te vergemakkelijken in een vraag en antwoord document. 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