{"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\/nl_nl\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/","title":{"rendered":"FDA stelt nieuwe vereisten voor tabaksproductenproductiepraktijken voor"},"content":{"rendered":"<p><span style=\"font-weight: 400;\">Op 10 maart 2023 publiceerde de Amerikaanse Food and Drug Administration een langverwachte voorgestelde regel over Requirements for Tobacco Product Manufacturing Practice, die voorgestelde vereisten voor de productie, het ontwerp, de verpakking en de opslag van tabaksproducten vastlegt. De voorgestelde vereisten zijn in wezen &quot;goede productiepraktijken&quot; voor tabaksproducten en zijn bedoeld om extra risico&#039;s die verband houden met dergelijke producten te minimaliseren en te voorkomen en zijn van toepassing op zowel binnenlandse als buitenlandse fabrikanten van afgewerkte en bulktabaksproducten.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Voor vape shops verduidelijkt de voorgestelde regel dat dergelijke vestigingen die alleen ENDS-producten en -componenten en -onderdelen verkopen, niet als fabrikanten worden beschouwd en niet onderworpen zijn aan de vereisten in de voorgestelde TPMP-regel, tenzij ze zich ook bezighouden met de productie, validatie van het ontwerp v\u00f3\u00f3r de productie, verpakking en opslag van afgewerkte of bulktabaksproducten in de zin van de regel.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Deze regel zou geen invloed hebben op &quot;kleine bedrijven gedurende 4 jaar na de ingangsdatum van de definitieve regel&quot;, maar het roept de vraag op... Hoeveel kleine vape-winkels verwacht de FDA nog steeds over 4 jaar en waarom de vertraging specifiek voor deze kleine bedrijven?\u00a0 <\/span><i><span style=\"font-weight: 400;\">De FDA definieert een klein bedrijf als een productfabrikant die maximaal 350 werknemers in dienst heeft.<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400;\">De FDA zal een openbare hoorzitting houden over\u00a0<\/span><b>12 april 2023<\/b><span style=\"font-weight: 400;\">, om opmerkingen te verzamelen van belanghebbenden, waaronder de industrie, de wetenschappelijke gemeenschap, belangenbehartigingsgroepen en het publiek. FDA zal ook een vergadering houden van het Tobacco Products Scientific Advisory Committee over\u00a0<\/span><b>18 mei 2023<\/b><span style=\"font-weight: 400;\">, om aanbevelingen te vragen van FDA&#039;s externe panel van experts over de vereisten die in de voorgestelde regelgeving zijn vastgelegd. Als onderdeel van de TPSAC-vergadering krijgt het publiek de gelegenheid om mondelinge presentaties te geven.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">U kunt zich aanmelden voor de openbare hoorzitting <\/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;\">hier<\/span><\/a><span style=\"font-weight: 400;\">; het evenement start om 9:30 uur en eindigt om 17:00 uur ET. De \u201c<\/span><span style=\"font-weight: 400;\">FDA wil van deze openbare hoorzitting een transparante en inclusieve gelegenheid maken om een scala aan idee\u00ebn en perspectieven van alle ge\u00efnteresseerde partijen te horen.\u201d Ik raad u daarom ten zeerste aan om u te registreren en te verzoeken om mondeling commentaar te leveren. Deze commentaren moeten uiterlijk 31 maart 2023 om 23:59 uur zijn ontvangen. Registratie voor alleen-luisteraars sluit op 12 april 2023 om 15:00 uur ET.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">\u2014\u2014-<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Om meer te horen over het komende nieuws en beleid rondom vapen, kunnen eigenaren van vape-winkels: <\/span><a href=\"https:\/\/worldvapersalliance.com\/nl_nl\/ambassador-program\/\"><span style=\"font-weight: 400;\">toepassen<\/span><\/a><span style=\"font-weight: 400;\"> aan het ambassadeursprogramma van WVA.<\/span><span style=\"font-weight: 400;\"> Door de WVA-ambassadeur te worden, hebben vape-winkels een unieke kans om lid te worden van een wereldwijd netwerk van vapers en in contact te komen met duizenden consumenten en activisten die hartstochtelijk vechten tegen schadelijk beleid dat een negatieve invloed zou hebben op hun rechten en bedrijven.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Vape-winkels zullen geen lid zijn van onze organisaties, maar als ambassadeurs kunnen ze onze gemeenschappelijke boodschap vermenigvuldigen: vapen redt levens.<\/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\/nl_nl\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:locale\" content=\"nl_NL\" \/>\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\/nl_nl\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:site_name\" content=\"World Vapers&#039; 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