{"id":3893,"date":"2023-03-22T08:06:45","date_gmt":"2023-03-22T12:06:45","guid":{"rendered":"https:\/\/worldvapersalliance.com\/?p=3893"},"modified":"2023-03-22T08:06:45","modified_gmt":"2023-03-22T12:06:45","slug":"fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices","status":"publish","type":"post","link":"https:\/\/worldvapersalliance.com\/it\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/","title":{"rendered":"La FDA propone nuovi requisiti per le pratiche di produzione dei prodotti del tabacco"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">Il 10 marzo 2023, la Food and Drug Administration statunitense ha pubblicato una proposta di norma, attesa da tempo, sui requisiti per le pratiche di fabbricazione dei prodotti del tabacco, che stabilisce i requisiti proposti per la fabbricazione, la progettazione, il confezionamento e lo stoccaggio dei prodotti del tabacco. I requisiti proposti sono essenzialmente &quot;buone pratiche di fabbricazione&quot; per i prodotti del tabacco e mirano a ridurre al minimo e prevenire i rischi aggiuntivi associati a tali prodotti e si applicano sia ai produttori nazionali che esteri di prodotti del tabacco finiti e sfusi.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Per i negozi di sigarette elettroniche, la norma proposta chiarisce che gli esercizi che vendono solo prodotti ENDS, componenti e parti non saranno considerati produttori e non saranno soggetti ai requisiti della norma TPMP proposta, a meno che non si occupino anche della fabbricazione, della convalida della progettazione pre-produzione, del confezionamento e dello stoccaggio di prodotti del tabacco finiti o sfusi ai sensi della norma.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Questa norma non avrebbe alcun effetto sulle &quot;piccole imprese per 4 anni dopo la data di entrata in vigore della norma definitiva&quot;, ma solleva una domanda: quanti piccoli negozi di sigarette elettroniche la FDA prevede che saranno ancora in attivit\u00e0 tra 4 anni e perch\u00e9 questo ritardo \u00e8 stato previsto proprio per queste piccole imprese?\u00a0 <\/span><i><span style=\"font-weight: 400;\">La FDA definisce una piccola impresa come un produttore di prodotti che impiega al massimo 350 dipendenti.<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400;\">La FDA ospiter\u00e0 un&#039;udienza pubblica su\u00a0<\/span><b>12 aprile 2023<\/b><span style=\"font-weight: 400;\">, per raccogliere commenti dalle parti interessate, tra cui l&#039;industria, la comunit\u00e0 scientifica, i gruppi di difesa e il pubblico. La FDA terr\u00e0 anche una riunione del Comitato consultivo scientifico sui prodotti del tabacco su\u00a0<\/span><b>18 maggio 2023<\/b><span style=\"font-weight: 400;\">, per ottenere raccomandazioni dal gruppo di esperti esterni della FDA sui requisiti stabiliti nella norma proposta. Nell&#039;ambito della riunione del TPSAC, il pubblico avr\u00e0 l&#039;opportunit\u00e0 di presentare relazioni orali.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u00c8 possibile registrarsi per l&#039;udienza orale pubblica <\/span><a href=\"https:\/\/www.eventbrite.com\/e\/fdas-proposed-new-requirements-for-tobacco-product-manufacturing-practices-tickets-570766466867\" target=\"_blank\" rel=\"noopener\"><span style=\"font-weight: 400;\">Qui<\/span><\/a><span style=\"font-weight: 400;\">; l&#039;evento inizier\u00e0 alle 9:30 e terminer\u00e0 alle 17:00 ET. Il &quot;\u201c<\/span><span style=\"font-weight: 400;\">La FDA mira a rendere questa udienza pubblica un&#039;opportunit\u00e0 trasparente e inclusiva per ascoltare una serie di idee e prospettive da tutte le parti interessate&quot;. Pertanto, consiglio vivamente di registrarsi e di richiedere commenti verbali; tali commenti devono pervenire entro il 31 marzo 2023 alle 23:59. Le registrazioni per i partecipanti in modalit\u00e0 solo ascolto si chiuderanno il 12 aprile 2023 alle 15:00 ET.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u2014\u2014-<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Per saperne di pi\u00f9 sulle prossime novit\u00e0 e politiche relative allo svapo, i proprietari di negozi di svapo possono <\/span><a href=\"https:\/\/worldvapersalliance.com\/it\/ambassador-program\/\"><span style=\"font-weight: 400;\">fare domanda a<\/span><\/a><span style=\"font-weight: 400;\"> al Programma Ambasciatori della WVA.<\/span><span style=\"font-weight: 400;\"> Diventando ambasciatori della WVA, i negozi di svapo hanno un'opportunit\u00e0 unica di entrare a far parte di una rete globale di vapers e di entrare in contatto con migliaia di consumatori e attivisti che combattono appassionatamente contro politiche dannose che influenzerebbero negativamente i loro diritti e le loro attivit\u00e0.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">I negozi di svapo non saranno membri delle nostre organizzazioni, ma come ambasciatori possono diventare moltiplicatori del nostro messaggio comune: lo svapo salva vite.<\/span><\/p>","protected":false},"excerpt":{"rendered":"<p>On March 10, 2023, the U.S. Food and Drug Administration published a long-awaited proposed rule on Requirements for Tobacco Product Manufacturing Practice which sets forth proposed requirements for the manufacture, design, packing, and storage of tobacco products. The proposed requirements are essentially \u201cgood manufacturing practices\u201d for tobacco products and are intended to minimize and prevent [&hellip;]<\/p>\n","protected":false},"author":15,"featured_media":3894,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[17],"tags":[],"class_list":["post-3893","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v28.1 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>FDA Proposes New Requirements for Tobacco Product Manufacturing Practices<\/title>\n<meta name=\"description\" content=\"On March 10, the FDA published a long-awaited proposed rule on Requirements for Tobacco Product Manufacturing Practice.\" \/>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/worldvapersalliance.com\/it\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:locale\" content=\"it_IT\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"FDA Proposes New Requirements for Tobacco Product Manufacturing Practices\" \/>\n<meta property=\"og:description\" content=\"On March 10, the FDA published a long-awaited proposed rule on Requirements for Tobacco Product Manufacturing Practice.\" \/>\n<meta property=\"og:url\" content=\"https:\/\/worldvapersalliance.com\/it\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:site_name\" content=\"World Vapers&#039; 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