Mandatory under Directive 2014/40/UE TPD-II [Art. 20(2)(b)].

The analysis includes 15 chemical parameters, indicated by the European Commission in accordance with EU Implementation Order 2015/2183 dated 24 November 2015. The vaporization is generated by a vaping machine, built conforming to ISO/DIS 20768 standard and compatible with every product on the market, thanks to a software that allows you to set specific analytical conditions..
In case of e-cigarettes or cartomizers sold in bundle with a specific e-liquid or a pre-filled device, the test is performed using the connected product. Otherwise we will use a 18 mg/ml nicotine neutral base or the liquid you’d like to (minimum 16 mg/ml nicotine strength).

To avoid additional requests from the authorities, we suggest performing the complete analysis set, but it’s possible for us to configure the parameter combinations you desire.
If your main market is UK, we suggest you follow the MHRA guidelines.

The available analyses are the following:

• titration of aldehydes (butirraldehyde, isobutirraldehyde, acrolein, acetaldehyde, propionaldehyde, crotonaldehyde, formaldehyde);
• volatile organic compounds – VOCs (diacetyl, 2,3 pentadione);
• titration of heavy metals (arsenic, cadmium, chromium, copper, lead, nickel).

The analyses are carried out by an accredited laboratory according to UNI CEI EN ISO/IEC 17025: 2005 standard.

Mandatory under Directive 2014/40/UE TPD-II [Art. 20(3)(b), (f)].

The nicotine release consistency testing is performed on the aerosol produced by the device using a vaping machine built conforming to ISO/DIS 20768 standard and compatible with every product on the market.
The test report presents the three emission points values ​​and the consistency assessment according to AFNOR standards.

In case of e-cigarettes or cartomizers sold in bundles with a specific e-liquid or a pre-filled device, the test is performed using the connected product. Otherwise we will use a 18 mg/ml nicotine neutral base or the liquid you’d like to (minimum 16 mg/ml nicotine strength).

The analyses are carried out by an accredited laboratory according to UNI CEI EN ISO/IEC 17025: 2005 standard.

Mandatory under Directive 2014/40/EU TPD-II [Ref. TPD Art. 20(9)].

We constantly confer with Member States to adopt the most compliant programs following the latest guidelines.
The first State requiring a description of the Health Surveillance Program is the United Kingdom through MHRA, the Authority responsible for the implementation of the TPD-II.