New European Commission guidance clarifies rodenticide user categories while allowing national flexibility under BPR provisions.
The European Commission has published guidance intended to create a common understanding of user categories for anticoagulant rodenticides and to support more consistent implementation of Mutual Recognition (MR) procedures across Member States.
The guidance describes three user categories:
While the guidance aims to support harmonisation, it also acknowledges that Member States may operate different national classification systems. Importantly, it confirms that countries can adapt user categories under Article 37 of the Biocidal Products Regulation (BPR) where justified on the grounds of protecting human health, animals or the environment.
From a Pelgar perspective, this guidance is particularly relevant as we continue to see a growing number of Member States stipulating trained professional user categories during MR applications, even where the reference authorisation contains broader professional user claims.
This development can have a significant impact on product positioning, label development and registration strategy across Europe. Manufacturers and authorisation holders seeking access to multiple European markets will need to consider how national interpretations of user categories may affect product approvals and commercial opportunities, despite the Commission’s efforts to encourage greater consistency across Member States.