For zero nic e-liquids with CBD, allowed in Austria and Estonia.

The notification process is conducted in accordance with EU Implementation Decision 2015/2183 of 24 November 2015, thanks to a mix of scientific, regulatory and IT competencies.

You can count on a dedicated personal assistant, who coordinates the whole process and become a unique and qualified referent for each request from and to each Member States.

All the documents concerning your notification process (analysis results, xml files, receipts, etc..) will be stored in a very safe dedicated section of our IT systems, shared with you to have your files always available.

We can carry out on your behalf the whole procedure, from the request for a Submitter ID to the submission of notifications through the EU-CEG of European Commission, or customizable according to your needs.
Notification service also includes the shipment of a notification declaration (with no legal value), the follow up with the European Commission and the Authorities of Member States of destination and the fully mediation and assistance in the event of requests from the Authorities.

In compliance with Reach Regulation (EC) No 1907/2006 and subsequent modifications, for all kind of CBD products.

The SDS is a legally binding informative document, the product supplier (manufacturer/importer/responsible company) must deliver to distributors or retailers (not to final users) when shipping the goods.

In order to ensure the confidentiality of your industrial secrets, SDS are issued by our own professionals and not by a third supplier. SDS are produced basing on of each single variant of flavour and nicotine, and in language of targeted market.

For all kind of CBD products.

We offer you all the testing to chacarcterize your products for a better approach to CBD regulations.

The analyses available are:

• Cannabinoid Profiling;
• Terpene Analysis;
• Heavy Metals;
• Pesticides;
• Mycotoxins.

For all kind of CBD products.

The regulatory elements to be included in the packaging of products with CBD are very different depending on the category in which the product falls; do you market a cosmetic or a medical device, or a supplement or novel food?

Rely on our support for:

• the definition of the regulatory elements to be included on the label (mandatory elements, nutritional table, claim …)
• the graphic studio.

In order to place a novel food on the market, a specific authorization must be requested from EFSA, the European Food Safety Agency, accordingly to Reg. (EU) 2015/2283.
Contact us for assistance in this specific path for your novel food with CDB!

Nowadays it is strategic to invest in high-quality R&D activities to raise the company competitiveness through the improvement of products and services.

Internal R&D capabilities can be developed learning extremely peculiar skills, that are not to be easily gained, beyond the installation of state-of-the-art technological equipments, that are often very expensive both in purchasing and maintenance.

These are the reasons why the ideal solution to optimize the results of an R&D activity, it’s to rely on a trusted partner, that can guarantee a strong skill background, and a solid history: we have what it takes!

Contact us to develop togheter your R&D project!