{"id":578,"date":"2020-10-13T16:47:48","date_gmt":"2020-10-13T16:47:48","guid":{"rendered":"https:\/\/www.farmalabel23.com\/servicios\/asuntos-regulatorios\/"},"modified":"2020-12-04T11:46:41","modified_gmt":"2020-12-04T11:46:41","slug":"regulatory-affairs","status":"publish","type":"page","link":"https:\/\/www.farmalabel23.com\/en\/services\/regulatory-affairs\/","title":{"rendered":"Regulatory Affairs"},"content":{"rendered":"[vc_row content_placement=”middle”][vc_column width=”2\/3″]
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Registration in the AEMPS Platforms<\/strong> to send documentation and maintenance of licenses<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Centralized Procedure:<\/strong> translation of national texts (SPC and PL), Blue Box national information for requesting a National Code, fractioning of texts for CIMA<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Decentralized Procedure and Mutual Recognition:<\/strong> translation of national texts, national phase with the AEMPS, approval of packaging materials, fractioning of texts for CIMA<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Variations<\/strong> of marketing authorizations: Quality, Safety and Efficacy<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Renewal<\/strong> of marketing licenses<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Processing<\/strong> and follow up with health authorities<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Readability Test<\/strong> and adaptation of texts to current legislation<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Scientific advice and Communication of Advertising<\/strong> to the CCAA authorities<\/h2><\/div><\/div>[vc_empty_space height=”20px”]
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Review of Promotional Material<\/strong><\/h2><\/div><\/div>[\/vc_column][vc_column width=”1\/3″][vc_single_image image=”632″][\/vc_column][\/vc_row]\n","protected":false},"excerpt":{"rendered":"

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