National Registration
Adjuvants
Tailor-made support for adjuvant registration across Europe. For more than 15 years, Redebel and RRA have specialized in this type of product and offer comprehensive assistance.
National Registration Support
Adjuvants have gained considerable traction on the European market. Until European Regulation 1107/2009 on adjuvants is implemented, registration applications are exclusively at national level.
Regulatory Services
- Strategic analysis and regulatory consulting: Analysis of data required (available and to be generated), national taxes, evaluation deadlines
- Stewardship: Preparation and participation for pre-application meetings
- Technical file drafting: Complete technical file and administrative documents
- Submission: Registration dossier to relevant authorities
- Monitoring: Efficient evaluation process and interactions with authorities
Laboratory & Field Support
- Laboratory studies: Support in conducting and monitoring of laboratory studies
- Efficacy trials: Setup across different countries through Redebel (Belgium) and Rhizome (Europe)
- Residue trials: Design and monitoring
- Spray drift tests: Specialized testing through Redebel
RRA prepares many national applications and also offers spray drift tests through Redebel.
With over 15 years of experience, we provide complete support for your adjuvant registration projects across Europe.
Continuous Training & Development
Ongoing training and regulatory monitoring ensure our team stays at the forefront of regulatory science.
120+
Training Hours / Year
15+
Conferences Attended
100%
Team Participation
Ready to Start Your Adjuvants Project?
Contact our adjuvants experts to discuss your specific national registration requirements and develop a strategic market access plan.