The Biocidal Products Directive requires that all biocidal products must as a general rule be authorised before they can be imported, placed on the market or used. During a transitional period when the EU is evaluating all active substances, some biocidal products will not be covered by the authorisation requirement.Products involved and responsibilityFind guidance on product-types in the legislation, registration requirements, borderline with other legislation, definitions and your obligations.When to apply An active substance can now fall within four categories with different consequences for the enterprises concerned - and your application. Find guidance on included and not included active substances in Annex I.How to apply Find guidance on application types, application forms, documentation requirements, fees etc.Evaluation of your application Find guidance on how the Danish EPA assess the effects on health, environment and efficacy. See caseprocessing times.
Requirements subsequent to the decision Find guidance on labels, classification, advertising, rapporting of sales etc.