PMTA (Premarket Tobacco Application) means that after
February 15, 2007, the legal listing of any new tobacco product requires FDA approval. The agency needs to consider whether this product is beneficial to public health.
After project preparation and research, WOOMI submitted a PMTA to the FDA before October 3, 2021.
Our product testing conducts scientific research and analysis in product analysis and manufacturing research, non-clinical research, clinical human research and other compliance fields.
Provide world-class quality and safe products
WOOMI digital factory established ISO9001:2015 and GMP820 quality management system, and invested millions of dollars to create a higher standard manufacturing environment and quality management system, which fully guarantee the standardized and intelligent management of design and development, product raw materials, production and manufacturing, product testing, quality control and other processes, and provide world-class quality experience.
WOOMI has always put product safety at the top of its list, and is committed to taking responsibility for the industry, users and society. And WOOMI has invested millions of dollars to prepare PMTA and will formally submit PMTA application to FDA before October 3, 2021.
PMTA is not an obstacle to the atomization industry, but a new starting point. WOOMI will continue to uphold the spirit of innovation, actively assume the responsibility of guardian of young adults, protect the health and safety of global consumer users, and promote orderly and good development of the industry. WOOMI will lead the market development with product and technology innovation in PMTA standards, and bring better life experience to global users.
Each WOOMI product needs to pass mechanical and physical properties, electrical, chemical properties and reliability tests, only to provide you with a professional, safe and great vape experience.