Regulatory Services for the Vape and Pharma Industry

We aim to deliver robust regulatory support allowing our clients to focus on growing their business.
Our broad experience with a range of products and clients enables us to proficiently address most regulatory challenges.
We offer expert regulatory advice that will bring your products to market without delay.

From the Knowledge Base:

Latest News:

6 Feb 2018, Public Health England states: “there is compelling evidence that e-cigarettes be made available to NHS patients.”. Read about the first medicinal e-cig here.

25 Oct 2017, UK Committee launch inquiry into e-cigs

28 Jul 2017, FDA extends PMTA submission deadline

20 May 2017, sale of non-compliant product deadline reached

20 Nov 2016, EU Tobacco Products Directive notification deadline reached

08 Aug 2016, FDA e-cigarette regulation takes effect

24 Jun 2016Brexit: UK votes to leave the EU

08 Jan 2016Results from the UK Public Consultation on Tobacco Products Directive implementation are published

06 Jan 2016, The first e-cigarette E-voke is licensed as a medicinal product

15 Dec 2015, Public consultation on local regulations ongoing in Norway

16 Oct 2015, Ireland’s Department of Health begin public consultation on domestic Tobacco Products Directive regulations


Join the Mailing List