Our Journey

Our Story

Thanks to its more than 30 years of experience and expertise, Redebel Regulatory Affairs (RRA) supports you in the approval process of plant protection and nutrition products, chemical substances (REACH) and biocides.

HomeOur Story

At Redebel, we began working as regulatory affairs consultants in response to one-off requests from customers who were performing pesticide efficacy trials and needed our help in completing their application.

These requests, like our profession, have evolved with the increasing complexity of legislation over the years. Redebel Regulatory Affairs - RRA, sister company of Redebel, was created in 2016 in view of the regulatory development of our different areas of activity.

Key Milestones

1990s - 2015

Foundation & Early Growth

Started as regulatory affairs consultants supporting customers with pesticide efficacy trials and regulatory submissions. Built expertise through one-off projects that evolved with increasing regulatory complexity.

2016

Birth of RRA

Redebel Regulatory Affairs - RRA was officially created as a sister company of Redebel in response to the regulatory development of different areas of activity. This marked our transition from consultancy to specialized regulatory firm.

2016 - Present

Continuous Growth

Our regulatory team has continued to grow in tandem with diverse regulatory changes across Plant Protection, Biocides, and REACH. Today we support clients across 40+ countries with 280+ successful dossiers delivered.

Regulatory Evolution

Our regulatory team has continued to grow over the years in tandem with diverse regulatory changes in different areas.

Plant Protection Products

→ Directive 91/414/EEC

→ Regulation (EC) 1107/2009

→ Adjuvants legislation

→ Fertilisers regulation

→ Biostimulants framework

Biocides

→ Directive 98/8/EC

→ Regulation (EC) 528/2012

→ Product authorization procedures

→ Active substance approval

→ Technical equivalence

REACH

→ Regulation (EC) 1907/2006

→ Registration deadlines (2010, 2013, 2018)

→ Substance evaluation

→ Authorization process

→ Ongoing compliance

Our Areas of Expertise

Our teams have developed areas of expertise in fields relating to regulatory sciences.

Ecotoxicology

Toxicology

E-FATE

BAD (Biological Assessment Dossier)

CLP Classification

Regulatory Strategy

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Our team will always propose the solution that best meets your needs and requests, while complying with the regulatory requirements laid down by the European Commission and National Authorities.

Inspired by nature, developed by experts.

Our Core Values

Respect

Quality

Confidentiality

Excellence

Discover Our Services

Learn how our expertise can support your regulatory needs across Europe and beyond.