Documents

1. What does professional or non-professional use mean for the authorisation of a biocide or plant protection product?

   In Article 71 (see below) the Plant Protection Products and Biocidal Products Act states that products authorised for ...

   Frequently asked questions

2. Am I permitted to use a lower dose than prescribed?

   This is only permitted for plant protection products; biocidal product must be used prescribed dosage.

   Frequently asked questions

3. What happens during a pre-submission meeting?

   During a Pre Submission Meeting the applicant receives procedural and substantive advice about the dossier that is to be ...

   Frequently asked questions

4. What is a pre-submission meeting (PSM)?

   A Pre Submission Meeting (PSM) is a consultation with a project leader and a number of experts that the Ctgb can organise at the ...

   Frequently asked questions

5. When is a product defined as a plant protection product?

   The European Regulation on plant protection products 1107/2009 uses the following definition: 'products, in the form that they ...

   Frequently asked questions

6. With a zonal application, will I automatically receive an authorisation for multiple EU Member States?

   No, but with a zonal application, authorisation in multiple Member States within the zone can be requested simultaneously. Before ...

   Frequently asked questions

7. When is a product on the market illegally or when is the use of a product illegal?

   Three situations can be distinguished in which a product is on the market illegally or the use of a product is illegal: A product ...

   Frequently asked questions

8. How can I obtain an authorisation for a plant protection product in another EU Member State?

   There are two possibilities: With a zonal application in the Netherlands (the Netherlands is ZRMS, zonal rapporteur Member ...

   Frequently asked questions

9. Can the Ctgb also reject an authorisation that is received through a mutual recognition procedure?

   Yes, rejection is possible based on Articles 36.3, 41.1, and 44 of 1107/2009/EC and Articles 11 and 12 of Directive 2009/128/EC.

   Frequently asked questions

10. According to the CLP, what are important data for labelling?

    Products which have been imported into or produced in the EU and delivered to a third party before June 1, 2015, are considered ...

    Frequently asked questions