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The March Conference

Join us at the European Regulatory Summit in Brussels this March. Our team will present the latest insights on biocide authorization pathways and cross-border compliance strategies. Book a meeting to discuss your regulatory challenges.

📍 Brussels, Belgium • March 15-17, 2026

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RRA at a Glance

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15+

Years of
Experience

14

Countries
supported

h

280+

Dossiers
Delivered

45+

Expert
Partners

R

98%

Client
Satisfaction

Products & Solutions

RRA provides expert regulatory consulting across five key product categories — from crop protection and biocontrol to specialty chemicals and industrial substances.

Plant Protection & Biocontrol

Full-spectrum regulatory support for conventional and biological crop protection — from active substance approval to multi-country product authorizations.

  • Active substance dossiers (Reg. 1107/2009)
  • Zonal & national product authorizations
  • Biopesticides & low-risk substance pathways
  • Mutual recognition & efficacy requirements

Plant Nutrition Solutions

Regulatory expertise for fertilizers, biostimulants, soil improvers and growing media under EU and national frameworks.

  • EU Fertilizing Products Regulation (2019/1009)
  • Biostimulant classification & dossiers
  • CE marking & national registrations
  • Organic & specialty product compliance

Adjuvants

Technical and regulatory support for adjuvants, safeners and synergists used alongside plant protection and agricultural products.

  • Substance registration dossiers (IUCLID)
  • SIEF participation & data sharing
  • Chemical Safety Reports (CSR)
  • Authorisation & restriction applications

Biocides

End-to-end regulatory services for biocidal products and active substances under EU Biocidal Products Regulation (528/2012).

  • Active substance approval (BPR Art. 7 & 11)
  • Union & national product authorizations
  • Same biocidal product & family applications
  • Product type strategy & dossier preparation

REACH

Comprehensive support for chemical substance registration, evaluation and authorisation under EU REACH Regulation (1907/2006).

  • Substance registration dossiers (IUCLID)
  • SIEF participation & data sharing
  • Chemical Safety Reports (CSR)
  • Authorisation & restriction applications

Where to find us

Meet Us at Upcoming Events

Connect with our team at key industry conferences across Europe. We attend regulatory summits, compliance workshops, and technical forums to share expertise and build partnerships.

Network & Integration

RRA operates through a coordinated network of local regulatory experts and technical partners across Europe and beyond. Our integration model ensures cross-border submissions are managed with consistent quality, aligned timelines, and effective authority interaction.

Cross-border coordination — Single point of contact for multi-country projects

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Consistent documentation — Standardised formats adapted to local requirements

Aligned timelines — Synchronised submissions and milestone tracking

Authority interactions — Local experts manage queries and follow-ups

In partnership with our sister companies, Redebel and Rhizome, we provide comprehensive, global management of your efficacy and residue trials.

Trusted by industry leaders

References & Testimonials

RRA has supported regulatory projects for leading agrochemical and specialty chemical companies worldwide. Our clients trust us to deliver compliant, high-quality dossiers on time.

After 10 years, still as responsive to requests and meticulous in their work. Thank you Thomas and thank you to your team.

With Studio Tum, I've had the opportunity to collaborate with Nic-nac on several projects (large and small format printing, vehicle lettering, sign placement, etc.). Each time, the service has been impeccable: responsiveness in management, quality of execution, and attention to detail. As a designer, it's a pleasure to be able to count on such a reliable and professional partner. I highly recommend them!

Great product, excellent responsiveness and communication. I highly recommend it.