Adact Medical Ltd (Adact) has over 20 years of medical product regulation experience across the world, that experience is brought to bear on the Tobacco Products Directive (TPD).

Adact provide a comprehensive TPD testing and submission service.
The TPD testing of e liquids and devices is just the beginning of the partnership with our customers.

As a one of our customers we will then support you by providing free advice and guidance on TPD packaging and labelling, Quality Management Systemsand direct support with MHRA queries or Trading Standards visits.

In addition to TPD testing and submission Adact also provide a comprehensive service for submitting vaping products under the FDA submission rules in the USA.

Our service provides our customers with simple access to all UK declared TPD products listed with the MHRA.

To find out more please fill in the contact us form at the bottom of the page.

We look forward to working with you.


At Adact Medical we fully understand the requirements for notifying a product under the Tobacco Products Directive and that registering is not the end of the journey. That is why we offer competitive rates across all  parts of the TPD process and ongoing maintenance of the regulatory responsibilities throughout the lifecycle of a vaping product.

It is this personal and approachable way of working that keeps our customers happy and confident in our services. Our help and advice does not end with notification; we also offer guidance with packaging, labelling, and localisation of products.

This is the reason why our customers keep coming back and why Adact Medical Ltd is a market leader in the vaping market*.