{"id":9459,"date":"2021-06-22T20:45:30","date_gmt":"2021-06-22T18:45:30","guid":{"rendered":"https:\/\/www.laffineur.com\/produits-pharmaceutiques\/"},"modified":"2021-06-22T20:52:09","modified_gmt":"2021-06-22T18:52:09","slug":"prodotti-farmaceutici","status":"publish","type":"page","link":"https:\/\/www.laffineur.com\/it\/prodotti-farmaceutici\/","title":{"rendered":"Prodotti farmaceutici"},"content":{"rendered":"

[vc_row rt_row_background_width=”fullwidth” rt_row_content_width=”default” rt_row_style=”default-style” rt_row_height=”” rt_column_gaps=”” rt_row_shadows=”” rt_col_anim=”true” rt_row_borders=”” rt_bg_effect=”classic” rt_bg_image_repeat=”repeat” rt_bg_size=”cover” rt_bg_position=”right top” rt_bg_attachment=”scroll” rt_bg_layer=”” rt_bg_video_format=”self-hosted” rt_class=”rt-3835284″ rt_paddings=”,,,” rt_margins=”,60,,” rt_content_margins=”,,,” rt_tablet_paddings=”,,,” rt_tablet_margins=”,,,” rt_tablet_content_margins=”,,,” rt_sp_paddings=”,,,” rt_sp_margins=”,,,” rt_sp_content_margins=”,,,” class=”text-justify”][vc_column width=”1\/2″ rt_bg_effect=”classic” rt_bg_image_repeat=”repeat” rt_bg_size=”auto auto” rt_bg_position=”right top” rt_bg_attachment=”scroll”]

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Prodotti Farmaceutici<\/h1>\n\t\t\t\t\t<\/div>[vc_column_text]L\u2019ottenimento di una autorizzazione all\u2019immissione sul mercato (AIM) di prodotti farmaceutici nell\u2019Unione europea risulta particolarmente complicato a causa di tre procedure distinte che si sovrappongono : l\u2019AIM nazionale, la procedura di mutuo riconoscimento e l\u2019AIM europea. A queste procedure va aggiunto l\u2019iter per la negoziazione dei prezzi e del rimborso dei medicinali, il quale \u00e8 sempre nazionale a prescindere dalla procedura di AIM.
\nIl nostro studio dispone di una solida esperienza nel campo della consulenza giuridica presso societ\u00e0 farmaceutiche nell\u2019ambito del completamento delle procedure sopra menzionate nonch\u00e9 delle tappe successive alle AIM, quale la farmacovigilanza.
\nSulla scia della sua competenza nell\u2019ambito del diritto farmaceutico, lo studio sta sviluppando una pratica nell’area del diritto dei pazienti.[\/vc_column_text][\/vc_column][vc_column width=”1\/2″ rt_bg_effect=”classic” rt_bg_image_repeat=”repeat” rt_bg_size=”auto auto” rt_bg_position=”right top” rt_bg_attachment=”scroll” rt_class=”rt-7592477″ rt_margins=”,” rt_paddings=”,,,” rt_wrapper_paddings=”,,,” rt_tablet_margins=”,” rt_tablet_paddings=”,,,” rt_tablet_wrapper_paddings=”,,,” rt_sp_margins=”,” rt_sp_paddings=”26,,,” rt_sp_wrapper_paddings=”,,,” rt_bg_color=”” rt_bg_overlay_color=””][vc_single_image image=”6389″ img_size=”full” alignment=”center”][\/vc_column][\/vc_row]<\/p>\n","protected":false},"excerpt":{"rendered":"

[vc_row rt_row_background_width=”fullwidth” rt_row_content_width=”default” rt_row_style=”default-style” rt_row_height=”” rt_column_gaps=”” rt_row_shadows=”” rt_col_anim=”true” rt_row_borders=”” rt_bg_effect=”classic” rt_bg_image_repeat=”repeat” rt_bg_size=”cover” rt_bg_position=”right top” rt_bg_attachment=”scroll” rt_bg_layer=”” rt_bg_video_format=”self-hosted” rt_class=”rt-3835284″ rt_paddings=”,,,” rt_margins=”,60,,” rt_content_margins=”,,,” rt_tablet_paddings=”,,,” rt_tablet_margins=”,,,” rt_tablet_content_margins=”,,,” rt_sp_paddings=”,,,” rt_sp_margins=”,,,” rt_sp_content_margins=”,,,” class=”text-justify”][vc_column width=”1\/2″ rt_bg_effect=”classic” rt_bg_image_repeat=”repeat” rt_bg_size=”auto auto” rt_bg_position=”right top” rt_bg_attachment=”scroll”][vc_column_text]L\u2019ottenimento di una autorizzazione all\u2019immissione sul mercato (AIM) di prodotti farmaceutici nell\u2019Unione europea risulta particolarmente complicato a causa di tre […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-9459","page","type-page","status-publish","hentry"],"yoast_head":"\nProdotti farmaceutici - 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