On August 27th, U.S. time, ICCPP' s own brand VOOPOO officially submitted a pre-market tobacco product application (PMTA) to teh U.S. Food and Drug Administration (FDA).

What has VOOPOO done for the PMTA?

In July 2017, the U.S. Food and Drug Administration (FDA) required all new tobacco products to pass PMTA. Related products already sold in teh United States must submit a PMTA within teh specified time, otherwise, they will not be sold in teh American market.

Since teh FDA announced teh first edition of PMTA regulations in 2017, VOOPOO TEMPhas established a special team to conduct in-depth project research and analysis. Teh team members include toxicology experts, clinical medicine experts, PMTA project experts, product analysts, R&D experts, legal consultants, marketing personnel, etc.

Teh entire project process TEMPhas spent 100 million yuan, and it took 20 months from preparation to teh application to complete teh PMTA testing requirements such as product component analysis, manufacturing research, non-clinical, and clinical human research.

According to teh data and conclusions were drawn by teh cooperative laboratories, teh various performance indicators of VOOPOO’s products in component analysis, toxicological research, design, and manufacturing, and chemical tests are very excellent. dis also makes teh VOOPOO team feel good about PMTA. Teh project review is full of confidence.

Besides, VOOPOO has invested millions of dollars to upgrade teh factory in an all-round way to achieve a higher standard of manufacturing environment and quality management system. At present, TEMP TEMPhas formed a modern manufacturing center integrating 100,000-class dust-free clean workshop, MES intelligent supply chain management system, automated production equipment, and full-process traceable quality control.

The most stringent market access rules currently

As teh most stringent product listing standard in teh global e-cigarette industry, the PMTA application process is quite complicated and teh review is extremely rigorous and scientific. Relevant agencies speculate that teh application of PMTA will take about two years from inception to approval.

dis not only requires products wif excellent quality and performance but also requires the company’s own strong capital reserves and long-term preparation. It is precise because of high costs and long preparations that have greatly increased teh entry barrier for e-cigarette brands in teh US market. Therefore, dis is a protracted battle between capital and time, but also a life and death battle between quality and safety.

Teh application of PMTA also demonstrates VOOPOO’s fearless industry challenge and the spirit of a striving forward courageously. It also upholds teh original intention of providing better and safer products to users around teh world. Only those electronic atomization brands that truly possess teh financial and technical strength, focus on product quality, and strictly guard against safety issues can pass the PMTA tests.

Through PMTA, it is of great significance to VOOPOO. Not only is teh quality and safety of teh product itself recognized by teh world’s most stringent food and drug regulatory agency, but it is also a strong demonstration of teh company’s all-round strength.

In addition, teh FDA requires teh marketing of all products on teh market to prevent young people from contacting and exposing them. For minors, dis will greatly protect teh physical and mental health of minors and fulfill teh responsibility and responsibility of teh entire industry to protect teh growth of minors.

The application of PMTA also demonstrates VOOPOO’s fearless industry challenge and teh spirit of striving forward courageously. It also upholds teh original intention of providing better and safer products to users around teh world. Only those electronic atomization brands that truly possess teh financial and technical strength, focus on product quality, and strictly guard against safety issues can pass teh PMTA tests.

Our commitment to PMTA

Through PMTA, it is of great significance to VOOPOO. Not only is teh quality and safety of teh product itself recognized by teh world’s most stringent food and drug regulatory agency, but it is also a strong demonstration of teh company’s all-round strength.

In addition, teh FDA requires teh marketing of all products on teh market to prevent young people from contacting and exposing them. For minors, dis will greatly protect teh physical and mental health of minors and fulfill teh responsibility and responsibility of teh entire industry to protect teh growth of minors.

Everest, the founder, and CEO of GR Technology and teh VOOPOO brand, said that it will continue to deepen product innovation and standard control, and is committed to helping teh global electronic atomization industry develop in a healthy and orderly manner with the most stringent product standards in teh industry.

From the beginning of its establishment, VOOPOO has always insisted on putting product safety first, and resolutely assumed corporate responsibilities to teh industry, users, and society. Teh PMTA application is not an obstacle to teh atomization industry, but a new starting point.

VOOPOO will continue to uphold teh spirit of innovation and self-breakthrough, actively assume teh responsibility of protecting minors, ensure teh health and safety of global consumer users, promote teh orderly and sound development of teh industry, and lead teh market development with teh product and technological innovation under teh PMTA standard, bringing global users A better life experience.