26/09/2024
Hi Kabarkadas!โบ๏ธ Ready for our ๐๐๐ ๐๐
๐๐๐ ๐๐๐? โ๏ธ ๐
๐๐๐๐๐๐๐๐๐ ๐๐๐๐๐ ๐๐. 106, ๐
๐๐๐ซ๐ฎ๐๐ซ๐ฒ 26, 2020
"PROHIBITING THE MANUFACTURE, DISTRIBUTION, MARKETING AND SALE OF UNREGISTERED AND/OR ADULTERATED ELECTRONIC NICOTINE/NON-NICOTiNE DELIVERY SYSTEMS, HEATED TO***CO PRODUCTS AND OTHER NOVEL TO***CO PRODUCTS, AMENDING EXECUTIVE ORDER NO. 26 (S. 2017) AND FOR OTHER PURPOSES."โ๏ธ๐
The World Health Organization (WHO) issued a report in August 2016 on Electronic Ni****ne and Non-Ni****ne Delivery Systems (ENDS/ENNDS), which noted that the use of adulterated and even unadulterated ENDS/ENNDS produces aerosol that ordinarily includes toxicants which trigger a range of significant pathological changes, and ENDS/ENNDS are unlikely to be harmless, such that long-term use is expected to increase the risk of chronic obstructive pulmonary disease, lung cancer, possible cardiovascuiar disease, as well as some other diseases associated with smoking.
โ๏ธ1. Prohibition of Unregistered and/or Adulterated ENDS/ENNDS, HTPs and Other Novel To***co Products. The manufacture, distribution, marketing or sale of unregistered or adulterated ENDS/ENNDS, components thereof in the form of devices, e-liquids, solutions or refills whether physically part of or intended to be used with ENDS/ENNDS, HTPs and other novel to***co products, are hereby prohibited and shall be dealt with in accordance with this Order and existing laws.
โ๏ธ2. Regulatory Framework for ENDS/ENNDS, HTPs and Other Novel To***co Products. All e-liquids, solutions or refills forming components of ENDS/ ENNDS or HTPs shall be registered with the FDA, in accordance with RA Nos. 9711 and 11467. All devices are forming components of ENDS/ENNDS or HTPs shall be subject to the product standards imposed by the FDA, in accordance with RA Nos. 7394 and 11467. Other novel to***co products shall be regulated in accordance with RA No. 9211 and other relevant issuances, and are subject to the jurisdiction of the Inter-Agency Committee-To***co (IAC-T), established under the said law.
โ๏ธ3. License to Operate. All establishments engaged in the manufacture, distribution, importation, marketing and sale of ENDS/ENNDS, HTPs, or their components, shall secure a License to Operate (LTO) from the FDA.
โ๏ธ4. Importation. The entry/importation of unregistered or adulterated ENDS/ENNDS, HTPs, or components thereof is hereby prohibited. For this purpose, the FDA and DTI are hereby directed to coordinate with the Bureau of Customs in the formulation of the guidelines, requirements and procedures for the regulation of the entry/ importation of ENDS/ENNDS, HTPs, and their components into the Philippine market.
โ๏ธ5. Implementing Guidelines. Within thirty (30) days from the effectivity of this Order, the FDA, in consultation with relevant agencies and stakeholders, shall formulate and issue the rules, regulations and standards governing the registration of ENDS/ENNDS, HTPs and their components, and the issuance of LTOs in relation thereto, required in this Order.
๐๐ป๐๐ปmore information about our law of the day๐๐ป๐๐ป
๐https://lawphil.net/executive/execord/eo2020/eo_106_2020.html?fbclid=IwZXh0bgNhZW0CMTEAAR3GPsN-UzTcP2fFvYkXLzFldW0aXSgg8ikjc-dSBUgxl5Jjgg3IyMWDHY4_aem_VnA69vjWfoTpuPSsmRV8og
KASAMA MO
SA PAGBABAGO
SA LABAN!