REGULATORY AFFAIRS

CONTROLLING INFORMATION 

 

 

 

 

 

The legislative framework pertaining to dietary supplements is still being erected in Europe and, as a result, many questions inevitably arise in the course of the product development process.

 

Our Regulatory Affairs Department is constantly monitoring the legislation in order to be able to provide you with practical advice now as well as helping you predict how the regulations may evolve in the future.

 

Tomorrow's regulations will weed out all but the best-structured and most accurately informed enterprises. And we are in a position to help you confront these challenges which are already looming up on the horizon (e.g. in the matter of novel active substances which have been licensed in the EU, rules on the justification of claims, etc.)

 

Finally, we maintain, close links with legislators and decision-makers in France with a view to defending our customers' interests and promoting the use of plants in consumer goods. We are also active in various bodies and commissions which have influence in determining the status of medicinal plants in France and in Europe.