The Applicant Guide Contents: Re-registration

Once an active substance has been approved under Article 80 of Regulation (EC) 1107/2009 (formerly known as inclusion in Annex I of Council Directive 91/414/EEC), Member States (MS) must re-evaluate plant protection products in accordance the Uniform Principles, on the basis of dossiers satisfying the active substance and product data requirements. We refer to this process as re-registration.

Please note that re-registration procedures do not apply to renewal of product authorisations in accordance with Article 43 of Regulation (EC) 1107/2009, which will be subject to separate procedures.

This section of The Applicant Guide provides information on:

• What is re-registration?
• General information on re-registration
• What you need to do at Step 1
• What you need to do at Step 2
• What else you need to consider for re-registration
• Extension of Use (Specific Off-Label Approvals)
• What you need to do if you are a parallel importer
• Application Overview for re-registration applications

Further information

• Re-registration deadlines and detailed supporting information for all active substances with an Annex I Inclusion date of 1 January 2009 (or later)
• Table of all active substance inclusions and their associated re-registration deadlines (2612kb)
• Information on the 'transitional arrangements'

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