Go to content
To the homepage of Board for the Authorisation of Plant Protection Products and Biocides
Home
Search
Frequently asked questions
Found 22 questions and answers about Biocides
Miscellaneous
Are products for human hygiene biocidal products, medical devices, pharmaceuticals or cosmetics?
Can data in the public domain be used?
Does a plant protection product or biocidal product have to be registered under REACH?
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 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 term 'expiration date' mean in the authorisation decision?
What is a biocidal product?
What is a pre-submission meeting (PSM)?
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 product defined as a biocidal 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 European biocidal product authorisations?
Will the fees and charges for applications be harmonised at the European level?
