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height=\"18.87\"><\/rect><rect x=\"565.43\" y=\"621.13\" width=\"28.54\" height=\"18.87\"><\/rect><rect x=\"59.66\" y=\"621.13\" width=\"28.54\" height=\"18.87\"><\/rect><\/svg> <\/div><div class=\"et-icon-content\"><\/div><\/div><\/div><p class=\"et-heading text-align-center highlight-false\" id=\"et-heading-458793\" data-374-f=\"26\" data-374-lh=\"36\" data-375-767-f=\"26\" data-375-767-lh=\"36\" data-768-1023-f=\"32\" data-768-1023-lh=\"40\"><span class=\"text-wrapper\"><span class=\"text\">Circa <span style=\"font-weight: 400;\">800 principi attivi<\/span> sono stati registrati in tutto il mondo per l&#8217;impiego nella protezione delle colture: un mercato in costante espansione legato alle crescenti richieste del settore agroalimentare.<\/span><span class=\"curtain\"><\/span><\/span><\/p><span class=\"et-gap et-clearfix et-gap-605660\"><\/span>[vc_column_text animation_delay=&#8221;0&#8243; css_animation=&#8221;none&#8221;]\n<p style=\"text-align: left;\">Prima che un PPP riceva l&#8217;autorizzazione da parte delle autorit\u00e0 competenti nei singoli stati per la commercializzazione, deve ricevere il permesso dall&#8217;Unione Europea.<\/p>\n<p style=\"text-align: left;\">La valutazione del principio attivo utilizzato \u00e8 un processo portato avanti sulla base di un Report dei dati raccolti:<br \/>\nL&#8217;EFSA analizza i suddetti documenti e presenta le sue conclusioni davanti ad un Comitato per l&#8217;industria alimentare e la salute animale, formato da esperti del singolo stato membro, il quale vota la sua approvazione all&#8217;impiego, attraverso dei processi armonizzati a livello Europeo e considerando fattori propri locali.<\/p>\n[\/vc_column_text]<span class=\"et-gap et-clearfix et-gap-4761\"><\/span>[\/vc_column][\/vc_row][vc_row gap=&#8221;0&#8243; element_id=&#8221;779700&#8243; element_css=&#8221;.vc-row-779700 .fixed-container {background-image:url(https:\/\/www.biotecnologiebt.it\/wp-content\/uploads\/green-apples-2021-08-26-17-13-48-utc.jpg);}&#8221; enable_first_overlay=&#8221;true&#8221; first_overlay_opacity=&#8221;25&#8243; first_background_color=&#8221;#a2c03a&#8221; fixed_bg=&#8221;true&#8221; css=&#8221;.vc_custom_1648057457526{border-top-width: 80px !important;border-bottom-width: 80px !important;padding-top: 60px !important;padding-bottom: 60px !important;}&#8221; fixed_bg_image=&#8221;4944&#8243;][vc_column animation_delay=&#8221;0&#8243; css_animation=&#8221;fadeIn&#8221; element_id=&#8221;903690&#8243; crp=&#8221;374:i:i,375-767:i:i,768-1023:i:i,1024-1279:i:i,1280-1599:i:i,1600-1919:i:i&#8221;][vc_empty_space height=&#8221;300&#8243;][\/vc_column][\/vc_row][vc_row][vc_column width=&#8221;1\/2&#8243;]<span class=\"et-gap et-clearfix et-gap-522880\"><\/span><p class=\"et-heading text-align-left highlight-false\" id=\"et-heading-1756\" data-374-f=\"26\" data-374-lh=\"36\" data-375-767-f=\"26\" data-375-767-lh=\"36\" data-768-1023-f=\"32\" data-768-1023-lh=\"40\"><span class=\"text-wrapper\"><span class=\"text\">Il nuovo Regolamento (EC)<br \/>\nN. 1107\/2009<\/span><span class=\"curtain\"><\/span><\/span><\/p><span class=\"et-gap et-clearfix et-gap-785761\"><\/span>[vc_column_text animation_delay=&#8221;0&#8243; css_animation=&#8221;none&#8221;]Il nuovo Regolamento (EC) N. 1107\/2009 \u00e8 entrato in vigore nel mese di Giugno 2011 e detta le nuove regole Europee per l&#8217;approvazione dei principi attivi e la loro commercializzazione nel mercato dei PPP.<\/p>\n<p>Le maggiori novit\u00e0 sono costituite da una regola di esclusione immediata in caso di sostanze pericolose, una procedura semplificata in caso di sostanze considerate di basso rischio e un&#8217;autorizzazione comunitaria per il mutuo riconoscimento e commercializzazione delle sostanze fra gli stati membri.<\/p>\n<p>Per facilitare quest&#8217;ultima, i territori Europei sono stati separati in 3 macro regioni con simili caratteristiche agricole, di salute e ambientali, cosicch\u00e9 l&#8217;autorizzazione concessa da uno stato sia automaticamente valida anche per gli altri inclusi nella zona di competenza.<\/p>\n<p><strong> Di seguito si pu\u00f2 esplorare una versione integrale della Normativa<\/strong>[\/vc_column_text]<span class=\"et-gap et-clearfix et-gap-533907\"><\/span><a id=\"et-button-422106\" class=\"et-button icon-position-left modal-false hover-none smooth-false shadow-false none round normal medium\" target=\"_blank\" href=\"https:\/\/www.biotecnologiebt.it\/download\/CRD_2015_Reg_1107_2009_C_F.pdf\" data-effect=\"none\"><span class=\"text\">Regolamento (EC) N. 1107\/2009<\/span><svg viewBox=\"0 0 220 56\" class=\"button-back\"><path class=\"regular\" d=\"M192,56H28A28,28,0,0,1,28,0H192A28,28,0,0,1,192,56Z\" data-hover=\"M192,56H28A28,28,0,0,1,28,0H192A28,28,0,0,1,192,56Z\"\/><\/svg><\/a>[\/vc_column][vc_column width=&#8221;1\/2&#8243;][vc_single_image image=&#8221;6002&#8243; 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La valutazione del principio attivo utilizzato \u00e8 un processo portato avanti sulla base di un Report dei dati raccolti: L&#8217;EFSA analizza<\/p>\n","protected":false},"author":2,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-vc.php","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/pages\/6440"}],"collection":[{"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/users\/2"}],"replies":[{"embeddable":true,"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/comments?post=6440"}],"version-history":[{"count":6,"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/pages\/6440\/revisions"}],"predecessor-version":[{"id":6680,"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/pages\/6440\/revisions\/6680"}],"wp:attachment":[{"href":"https:\/\/www.biotecnologiebt.it\/it\/wp-json\/wp\/v2\/media?parent=6440"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}