Protection & nutrition Adjuvants
Adjuvants have gained considerable traction on the European market. For more than 15 years, Redebel and RRA have been working on this type of product and offer tailor-made support.
Until European Regulation 1107/2009 on adjuvants is implemented, registration applications are exclusively at national level.
Strategic analysis and regulatory consulting
Analysis of the data required (available and to be generated), national taxes, evaluation deadline
Stewardship (preparation and participation) for pre-application meetings
Drafting of the technical file and administrative documents
Support in conducting and monitoring of laboratory studies
Support in setting up efficacy and residue trials in different countries depending on the specificities of your adjuvants through our company Redebel for trials in Belgium and through Rhizome for European projects
Submission of the registration dossier to relevant authorities
Efficient monitoring of the evaluation process and interactions with relevant authorities
RRA prepares many national applications and also offers spray drift tests through Redebel.