Medic Pro LimitedBusiness Consultant in London

Business Details
We are a European Regulatory Affairs Consultancy. We help pharmaceutical companies obtain medical licences for their products. We also advise electronic cigarette companies on the emerging regulations. E-cigarette Industry With e-cigarette regulation still in development, there are no official guidelines or standards. In their absence, pharmaceutical regulatory guidelines can be used as a model. Our knowledge and experience in pharmaceutical regulatory affairs combined with knowledge on the latest developments in e-cigarette regulatory activity allows us to help manufacturers prepare early. We offer a range of services that span e-cigarette regulation and manufacturing standards. More specifically, we help companies to: - Source cost-effective emissions testing laboratory - Comply with the 'leakage-free' product requirements - Conduct shelf life testing on e-liquids and devices Visit our website for more information:
Business Details
  • Website:
  • Servicing commercial and industrial clients
  • Insured
  • Year established: 2010
Highlights, Specialties & Features
  • TPD Testing
  • TPD compliant
  • e-liquid testing lab
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Contact Details
49 Brixton Station Road
map & driving directions
Phone Number
+44 (0)20 3411
Products & Services
Pharmaceutical Industry
Registration of a Medicinal Product

Life-Cycle Maintenance

Dossier Conversions

Due Diligence

eCTD Publishing

Management, Supervision and Training
E-cigarette Regulations
The Tobacco Products Directive 2014/40/EU lays down the rules for the manufacture, presentation and sale of e-cigarettes.  It came into effect on 20th May 2016.

A number of restrictions are placed on products such as a limit on nicotine concentration (≤20 mg/ml) and tank volume (≤2 ml).  Also, under the new rules a pre-market notification is required. Certain information on the product must be submitted to the authorities at least 6 months before a product can be placed on the market.  The information to be submitted includes administrative, quality and safety data and will require emissions testing by an analytical laboratory and a toxicological assessment.

The new regulations have a significant impact on business, bringing new costs and major changes in operations.
Client Testimonials
Testimonial #1
The regulatory support we received over the past 2 years has been fantastic. It has been professional and reliable and the best we’ve found. From assisting us with the notifications to e-liquid testing they’ve helped get us TPD compliant and even saved us money.

We will continue to get their advice on all regulatory matters.
BySam (E-liquid Manufacturer)
Testimonial #2
Medic Pro really helped to alleviate the pressure caused by the TPD. We import products from China and getting the necessary assurances [as a result of the TPD] was sometimes difficult. Medic Pro supported us to make sure we were meeting our commitments. They also gave us confidence that whatever compliance issue might arise – with their support – it could be dealt with.

We’re very satisfied with the service and more than happy to recommend them.
ByFred (UK importer/retailer)
Testimonial #3
Without a doubt, they are an invaluable source of regulatory information. We always make time to hear what they have to say.
ByM. D. (UK Manufacturer/Distributor)
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+44 (0)20 3411
Hours of Operation
Monday09:00 AM÷06:00 PM
Tuesday09:00 AM÷06:00 PM
Wednesday09:00 AM÷06:00 PM
Thursday09:00 AM÷06:00 PM
Friday09:00 AM÷06:00 PM
Saturday11:00 AM÷04:00 PM
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