{"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_be\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/","title":{"rendered":"FDA stelt nieuwe eisen voor de productiepraktijken van tabaksproducten voor."},"content":{"rendered":"<p><span style=\"font-weight: 400;\">Op 10 maart 2023 publiceerde de Amerikaanse Food and Drug Administration (FDA) een langverwacht voorstel voor regelgeving betreffende de productiepraktijken van tabaksproducten. Dit voorstel bevat voorgestelde eisen voor de productie, het ontwerp, de verpakking en de opslag van tabaksproducten. De voorgestelde eisen zijn in wezen &quot;goede productiepraktijken&quot; voor tabaksproducten en zijn bedoeld om extra risico&#039;s die met dergelijke producten gepaard gaan te minimaliseren en te voorkomen. Ze zijn van toepassing op zowel binnenlandse als buitenlandse fabrikanten van afgewerkte en bulktabaksproducten.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Voor vapeshops verduidelijkt de voorgestelde regelgeving dat dergelijke bedrijven die uitsluitend ENDS-producten en -onderdelen verkopen, niet als fabrikanten worden beschouwd en niet onderworpen zijn aan de eisen van de voorgestelde TPMP-regelgeving, tenzij zij zich ook bezighouden met de productie, de validatie van het ontwerp in de voorproductie, het verpakken en de opslag van afgewerkte of bulktabaksproducten in de zin van de regelgeving.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Deze regel zou geen gevolgen hebben voor &quot;kleine bedrijven gedurende 4 jaar na de ingangsdatum van de definitieve regel&quot;, maar roept wel de vraag op... Hoeveel kleine vapewinkels verwacht de FDA dat er over 4 jaar nog steeds bestaan en waarom wordt deze regel juist voor deze kleine bedrijven uitgesteld?\u00a0 <\/span><i><span style=\"font-weight: 400;\">De FDA definieert een klein bedrijf als een productfabrikant met 350 werknemers of minder.<\/span><\/i><\/p>\n<p><span style=\"font-weight: 400;\">De FDA organiseert een openbare hoorzitting 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, belangenorganisaties en het publiek. De FDA zal ook een bijeenkomst houden van het Wetenschappelijk Adviescomit\u00e9 voor Tabaksproducten.\u00a0<\/span><b>18 mei 2023<\/b><span style=\"font-weight: 400;\">, om aanbevelingen te vragen aan het externe panel van deskundigen van de FDA over de eisen die in de voorgestelde regelgeving zijn vastgelegd. Tijdens de TPSAC-bijeenkomst 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 begint om 9:30 uur en eindigt om 17:00 uur ET. De\u201c<\/span><span style=\"font-weight: 400;\">De FDA wil van deze openbare hoorzitting een transparante en inclusieve gelegenheid maken om een scala aan idee\u00ebn en perspectieven van alle belanghebbenden te horen. Daarom raad ik u ten zeerste aan om u te registreren en een verzoek in te dienen om mondeling commentaar te geven. Deze reacties moeten uiterlijk 31 maart 2023 om 23:59 uur binnen zijn. Registratie voor deelnemers die alleen willen luisteren 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 weten te komen over het aankomende nieuws en beleid rondom vapen, kunnen eigenaren van vapewinkels contact met hen opnemen. <\/span><a href=\"https:\/\/worldvapersalliance.com\/nl_be\/ambassador-program\/\"><span style=\"font-weight: 400;\">toepassen<\/span><\/a><span style=\"font-weight: 400;\"> naar het ambassadeursprogramma van WVA.<\/span><span style=\"font-weight: 400;\"> Door ambassadeur te worden van de WVA (Women&#039;s Vape Association), krijgen vapewinkels een unieke kans om zich aan te sluiten bij een wereldwijd netwerk van vapers en in contact te komen met duizenden consumenten en activisten die zich vol passie verzetten tegen schadelijk beleid dat hun rechten en bedrijven negatief zou be\u00efnvloeden.<\/span><\/p>\n<p><span style=\"font-weight: 400;\">Vapewinkels zullen geen lid zijn van onze organisaties, maar als ambassadeurs kunnen ze onze gezamenlijke boodschap verspreiden: 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_be\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:locale\" content=\"nl_BE\" \/>\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_be\/fda-proposes-new-requirements-for-tobacco-product-manufacturing-practices\/\" \/>\n<meta property=\"og:site_name\" content=\"World Vapers&#039; 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