Registration of Adjuvant in Europe with specific focus on France and Belgium
This webinar provides an overview of adjuvant legislation, with a focus on national requirements and applicable technical obligations. It will also highlight the regulatory and technical specificities of adjuvants particularly in France and Belgium, in comparison with plant protection products, to clarify key challenges and points of attention for their placement on the market.
The topic of adjuvant efficacy will not be covered in this webinar, as a webinar dedicated to this topic is already available.
Objectives and skills
To understand the regulatory framework applicable to adjuvants at both European and national levels, as well as the associated technical requirements, in order to better anticipate regulatory expectations and address the specificities of these products.
Public and prerequisites
- Any actors needing to understand the basics of adjuvant registration.
- No specific adjuvant knowledge is required to attend the webinar.
Program/Content
- What is an adjuvant? (Definitions & legislations)
- Overview of adjuvant dossier registration in Europe
- How to build adjuvant dossiers in FR and BE: national requirements and Tips & Trics
Details and technical aspects
- Date : 01 Octobre 2026
- Training duration: +/-1h30
- Time : 9h30-11h00
- Language of presentation : English
- Language of training material : English
- Online Training
- Cost: 350€
- Minimum number of participants : the training will be held based on a minimum of 5 participants.
- Participation fee is for ONE participant (Fees are to be paid individually for each participant).
- A 10% discount will be applied to the price from the second participant from the same company in the same training. Please register the first participant and contact rraacademy@redebel.com to receive the promocode.