Device manufacturing standards
Committed to manufacturing excellence
As a company dedicated to therapeutic nicotine vaping, we uphold the highest manufacturing and safety standards to ensure can trust the quality, safety, and compliance of our products. Our manufacturing partner goes beyond globally recognized quality and medical device standards with additional certifications that set us apart.
Industry-Recognized Quality Standards
ISO 9001: Internationally recognized quality management system, ensuring consistent, high-quality production.
ISO 13485: Medical device-specific quality standard, providing additional safety and regulatory compliance.
cGMP: (Current Good Manufacturing Practice) Pharmaceutical-grade quality, safety, and efficacy assurance.
Our Unique Standards for Safety, Ethics & Sustainability
HACCP: Hazard Analysis & Critical Control Points, a gold standard in risk assessment for product safety.
ISO 14001: Environmental responsibility, reducing waste and promoting sustainability in manufacturing.
ISO 45001: Occupational health & safety compliance, prioritizing worker well-being and safe production environments.
SA 8000: Ethical and socially responsible manufacturing, ensuring fair Labor practices and worker protection.
By exceeding standard requirements, we provide a therapeutic nicotine solution that is produced with uncompromising quality, safety, and ethical responsibility.
Device and Battery standards
Certified for Safety
Our therapeutic nicotine vaping devices meet the highest international safety and compliance standards to guarantee electrical safety, environmental responsibility, and regulatory compliance.
Our Device Certifications:
FCC: Electromagnetic safety standards, preventing interference with medical and electronic devices.
CE: EU health, safety, and environmental protection requirements for consumer safety.
RCM: Australian compliance with electromagnetic compatibility regulations.
RoHS: Restricts hazardous substances, ensuring free from harmful materials like lead and mercury.
IEC 60335-1: Global standard for electrical safety, ensuring devices meet stringent reliability and durability requirements.
IEC 62133-2: Battery safety, reducing risks of overheating, leakage, or malfunction.
UN38.3: Ensuring compliance with international shipping and handling regulations.
With these certifications, you can trust that our devices meet the highest standards of safety, quality, and compliance, supporting harm reduction with reliable, thoroughly tested technology.
E-Liquid product standards
Manufactured to the highest standards
Our liquids are manufactured in state-of-the-art facilities that adhere to the highest international quality and safety standards, including cGMP (Current Good Manufacturing Practice), HACCP (Hazard Analysis and Critical Control Points), and ISO 9001 certifications.
While not a specific requirement under TGO 110, these rigorous certifications underscore our commitment to product safety, consistency, and pharmaceutical-grade quality.
By exceeding baseline regulatory requirements, we provide the market with greater confidence in the reliability and purity of our formulations. This proactive approach to compliance and safety aligns with the professional standards expected in therapeutic product dispensing, ensuring that patients receive a product that meets the highest benchmarks for quality assurance
Our liquid formulations are developed with pharmaceutical precision, ensuring full control over ingredient composition at a molecular level. This meticulous approach allows us to eliminate HPHCs (Harmful and Potentially Harmful Constituents), volatile organic compounds, aldehydes, and other contaminants linked to toxicity and carcinogenicity.
By exclusively using US and EU Pharmacopoeia-grade Propylene Glycol, Vegetable Glycerin, and Nicotine, we maintain the highest standards of purity, consistency, and compliance.
This commitment to ingredient integrity not only aligns with therapeutic product safety expectations but also provides confidence in dispensing a product that prioritizes patient safety, regulatory adherence, and clinical reliability.
Only the highest quality ingredients
Tested for compliance and quality
Each batch of our vape liquids undergoes comprehensive analytical testing in independent ISO 17025 certified labs to ensure compliance with the highest pharmaceutical and toxicological standards.
We systematically assess nicotine concentration, prohibited and contaminant substances, microbial presence, aldehydes, and Vitamin E Acetate, with internal acceptance criteria set at non-detect levels with any trace detection results in batch rejection.
Furthermore, we conduct toxicological evaluations, including studies on toxicity, carcinogenicity, and mutagenicity, to assess the potential biological impact of all ingredients.
This stringent quality control framework ensures that pharmacists can dispense with confidence, knowing that our products meet rigorous safety, purity, and regulatory benchmarks aligned with therapeutic and clinical best practices.
Achieving lowest emissions
Precision-Engineered for Minimal Emissions
Minimizing emissions is at the core of our product design. Through stringent manufacturing protocols, pharmaceutical-grade formulations, advanced technology, and rigorous testing, we deliver a product with the lowest possible emissions, prioritizing patient safety and regulatory compliance.
Manufacturing Standards
Ingredient Standards
Advanced Coil Technology
Aerosol testing
Produced in cGMP, ISO 13485, and ISO 9001-certified facilities, ensuring pharmaceutical-grade quality, consistency, and purity.
Formulations defined at a molecular level, allowing precise ingredient control, Only Pharmacopoeia-grade PG, VG and Nicotine are used, free from HPHCs, aldehydes, VOC, and carcinogenic contaminants, eliminating impurities, inconsistencies and exposure to known toxicants.
Medical-grade stainless steel heating system ensures a cleaner, larger uniform heating surface for temperature stability. Paired with precise temperature control technology, liquids are vapourised at a Low (195°C) temperature minimizing thermal degradation and emission of harmful byproducts.
Aerosols are tested in Independent ISO 17025 certified laboratories for Carbonyl compounds, Metals, Glycols, Nitrosamines, VOC substances, Diacetyl and Pentane 2,3 dione, with a Non-Detect standard
By integrating pharmaceutical-grade standards with precision engineering, our NVPs set a new benchmark in emission reduction
Consumer Medicinal Information (CMI)
User Manuals
Any questions? Contact us…
Email: info@teamftf.com
Phone: 1300 926 540