Medic Pro Limited

Business Consultant in London
Business Consultant in London 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: www.medicpro.london/tobacco-products-directive
Business Details
  • Serving commercial and industrial clients
  • Insured
  • Year established: 2010
Highlights & Specialties
  • TPD Testing
  • TPD compliant
  • e-liquid testing lab
Social Profiles

Contact Details

Address
49 Brixton Station Road
London
SW9 8PQ
Phone
Driving Directions

Products & Services

Pharmaceutical Industry
read moreRegistration of a Medicinal Product

Life-Cycle Maintenance

Dossier Conversions

Due Diligence

eCTD Publishing

Management, Supervision and Training

E-cigarette Regulations
read moreThe 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.

Testimonials

Sam (E-liquid Manufacturer)
read moreThe regulatory support we received over the past 2 years has been fantastic. It has been professional and reliable and the best weve found. From assisting us with the notifications to e-liquid testing theyve helped get us TPD compliant and even saved us money.

We will continue to get their advice on all regulatory matters.

Fred (UK importer/retailer)
read moreMedic 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.

Were very satisfied with the service and more than happy to recommend them.

M. D. (UK Manufacturer/Distributor)
read moreWithout a doubt, they are an invaluable source of regulatory information. We always make time to hear what they have to say.
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
SundayClosed
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