Globally respected and trusted regulatory compliance to support the electronic cigarette and vaping industry since the introduction of the very first products in the early 00’s
Scientists helping to build businesses
ADACT Medical Ltd brings together over 20 years’ experience of medical product regulatory compliance within the pharmaceutical, biotechnology, medical devices, herbal medicines and supplements sectors.
Your trusted experts
Our founder and Chief Regulatory Officer is Damien Bové BSc (Sci. Hons), MSc (Sci. Open), RICR who today leads a team of experts who have an in-depth knowledge and appreciation of the rapidly growing electronic cigarette, vaping and CBD industries.
Customer focused
Whether you are a new brand in need of some assistance or one of our biggest international customers, we put every customer at the heart of everything we do.
4 May 2021
After a successful launch, the rollout of New Zealand’s Smokefree Environments and Regulated Products (Vaping) Amendment Act is well underway with further changes coming into force on 11 May 2021. The Act which passed on 11…
30 April 2021
ADACT have received clarification on General Enforcement Discretion Related to Sept. 9 Premarket Tobacco Applications from the FDA. We received the following on 29 April 2021. “Per a court’s order, for new deemed tobacco products…
10 March 2021
Following the UK leaving the European Union on 1 January 2021, cosmetic products – including those with CBD or hemp based ingredients – require re-registering. If you make cosmetic products, which are available to consumers in…
14 February 2021
The concept of e-cigarette and vape products acting as a method of COVID-19 transmission has been discussed many times since the pandemic arrived in 2020. The respiratory flow associated with vaping is visible (as opposed to other…
8 February 2021
The Department of Health and Social Care (DHSC) is carrying out a public consultation regarding The Tobacco and Related Products Regulations 2016 (TRPR) and The Standardised Packaging of Tobacco Products Regulations 2015 (SPoT).
4 February 2021
The U.S. Food and Drug Administration (FDA) displayed the final rule for the Premarket Tobacco Product Application (PMTA) in the federal register, but it did not get published on 19 January 2021. A day later on 20 January, a memo from The…