Go to content
Home
Search
Frequently asked questions
Found 41 questions and answers
Miscellaneous
Am I permitted to use a lower dose than prescribed?
Are biostimulants and growth regulators classified as plant protection products?
Are products for human hygiene biocidal products, medical devices, pharmaceuticals or cosmetics?
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?
FAQ's on important changes to the CLP Regulation
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 can I see whether a biocidal product is authorised?
How do I introduce a biocide on the Dutch market?
How do I obtain an authorisation for my biocidal product in more than one Member State?
How does Europe ensures pesticides are safe?
How does the Ctgb deal with data protection?
How does the Ctgb define data in the public domain?
Is my disinfectant product a biocidal product or a veterinary/medicinal product?
Is there a difference between professional and private use of a biocidal product?
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 biocidal product?
What is a pre-submission meeting (PSM)?
What is the CTGB VAT-number?
What is the importance of a Letter of Access (LoA) when submitting data?
When a product is intended for disinfection of medical instruments and falls under legislation for medical devices, should it also have an N number? Or is a CE number sufficient?
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 biocidal product?
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)?
Where can I find the list of active substance dossiers included in the review programme?
Where can I find the list of European biocidal product authorisations?
Where can I go with my questions about treated articles?
Where do I find the list of approved suppliers? (BPR article 95 list)
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?
