Biocides

Our competences for biocidal registration

A complete support for registration:

• Preliminary analysis of your needs

• Definition of an adapted strategy

• Identification of key studies

• Close contacts with Authorities

National submission (in all EU countries):

• Following transitional period procedure

• Post-Inclusion procedure

• Label preparation, MSDS, other administrative documents, in collaboration with specialised and certified translators

EU Review Program / New active substance:

• Product evaluation and Data Gap Analysis

• Discussions with RMS to establish an adequate and specific registration strategy (case by case approach)

• Compilation of the Dossier (Annex IIA and IIB): summary of studies, compiling of documents, building of the dossier

• IUCLID5

• Submission and follow-up of the dossier until successful inclusion/authorisation

• Project management of complete dossier with our network of collaborators

Post-inclusion support:

• Product dossier preparation in EU standard format

• Choice and contact the adequate RMS

• Mutual recognition applications in 27 Member States

National notifications and “non-regulated biocides”