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Frequently asked questions

Found 25 questions and answers about Plant Protection Products

  • Miscellaneous

    • Am I permitted to use a lower dose than prescribed?
    • Are biostimulants and growth regulators classified as plant protection products?
    • Can CA reports in the public domain be used without proof of ownership
    • Can data in the public domain be used?
    • Can the Ctgb also reject an authorisation that is received through a mutual recognition procedure?
    • Does a plant protection product or biocidal product have to be registered under REACH?
    • Generic plant protection product in the Netherlands (article 34)
    • Has the Definition list scope of permitted use (DTG list) been harmonised at the European level?
    • How can I obtain an authorisation for a plant protection product in another EU Member State?
    • How does the Ctgb deal with data protection?
    • How does the Ctgb define data in the public domain?
    • What does professional or non-professional use mean for the authorisation of a biocide or plant protection product?
    • What does the Ctgb consider to be a reliable endpoint?
    • What does the term 'expiration date' mean in the authorisation decision?
    • What happens during a pre-submission meeting?
    • What if a maximum residue limit has not yet been established?
    • What is a pre-submission meeting (PSM)?
    • What is the importance of a Letter of Access (LoA) when submitting data?
    • When is a certificate of professional competence required?
    • When is a delivery and run-down period (grace period) granted?
    • When is a product defined as a plant protection product?
    • When is a product on the market illegally or when is the use of a product illegal?
    • When is an exemption granted for a product (plant protection product or biocidal product)?
    • Will the fees and charges for applications be harmonised at the European level?
    • With a zonal application, will I automatically receive an authorisation for multiple EU Member States?

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