Vape & TPD services

Ensuring compliance and testing for vaping products.

Compliance for vape products

Vaping products must comply with the European Tobacco Products Directive 2014 (TPD2), the UK Tobacco and Related Products Regulations 2016 (TRPR), U.S. Premarket Tobacco Product Application (PMTA) and other safety regulations to ensure consumer safety. ADACT Medical provides comprehensive testing and compliance services to help you meet these strict requirements and maintain consumer trust.

Essential services

TPD QA and QC Testing
TPD registration & Testing

TPD registration & testing

Full compliance with TPD and TRPR, including emissions testing and toxicology reports.

Labelling & safety data sheets

Safety data sheets (SDS) and Poisons Centre Notifications (PCN) are a legal requirement for vaping and many other products.

TPD stability storage and analysis

Quality Assurance testing

 Includes 2ml fill level, nicotine potency and diketones.

Stability storage & analysis

Assessing product shelf life and quality over time.

As one of the major influencers of the Tobacco Products Directive (TPD), we've become a leading provider of regulatory consultancy services in the UK, Europe, the Middle East, China, North America and New Zealand.

For nearly a decade, ADACT Medical has enabled vapes businesses to bring their products to market smoothly and meet full TPD compliance.

Beyond consultancy, our founder Damien Bové represents the industry on the British Standards Institute (BSI) committee, UKVIA, and is a member of the Institute of Clinical Research (ICR), keeping us ahead in vaping regulations.

Work with the vape experts

Work with vape experts

Our full range of TPD & TRPR services

ADACT Medical full range of TPD and TRPR services

ADACT Medical's commitment to scientific innovation

ADACT Medical prides itself on being at the forefront of scientific innovation. Our state-of-the-art lab is equipped with the latest technology, allowing us to tackle complex testing challenges with precision and accuracy.

ISO/IEC 17025:2017 accredited:
Ensuring high standards of quality and accuracy.

Advanced equipment:
Including HPTLC, HPLC, GC-MS, and LC-MS for comprehensive testing capabilities.

Continuous improvement:
We constantly update our methods and equipment to stay ahead in the industry.

Key benefits

Expertise in TPD & vaping compliance:
Our team specializes in navigating complex regulatory landscapes.

Quick turnaround times:
We understand the importance of timely results for product development.

Transparent reporting:
Providing detailed reports to support your compliance efforts and product development.

Contact ADACT Medical for all your TPD compliance needs

Ready to ensure the compliance and safety of your vaping products? Contact us today to discuss your testing needs and learn how we can help.

 FAQs

  • We test a wide range of vaping products, including e-liquids, devices, pens, pods, and more. We can customise our testing approach to meet your specific needs.

  • Our standard turnaround time is 5-10 working days, depending on the specific tests required. We also offer expedited services for urgent testing needs.

  • ADACT Medical's laboratory is ISO/IEC 17025:2017 accredited, providing rigorous quality and accuracy standards.