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The Registration Process
Full details on how to submit an application are given in:
We also have an:
Approval and review of active substances in the EU
Guidance on how to go about applying for approval of a new active substance via the EU process, along with guidance about the Review of existing active substance is included in the Applicant Guide.
Fees for Applications
Information on CRD Fees charged for individual application types is available at the following link
Details of the data requirements for approval of active substances in the EU and authorisation of products in the UK, as well as guidance documents, are given in our Data Requirements area.
Classification and Labelling guidance
Guidance on classification and labelling of products is given in our Labelling Handbook.
See a list of application forms on the following page: