The Applicant Guide: UK Guidance
The UK has left the EU, new rules from January 2021
The transition period after Brexit comes to an end this year.
The Applicant Guide provides guidance on the procedures for submitting an application to CRD, how we will process the application, what should be included in an application and what happens once the application is completed.
In addition to the Guide there is UK guidance which addresses different aspects of pesticide and adjuvant registration. Links to these documents can be found in the appropriate places in The Applicant Guide but a list of these documents is also detailed below.
The Applicant Guide associated UK Guidance
Active Substance Approval – The EU Decision Making Process
New Active Substances applications – optional phased submission process
Additional data and data mid-evaluation
Adverse data - Approval Holder Responsibilities
Applications for addition of undersown crops to product labels
Classification and labelling requirement on authorisations issued after 14 June 2011
Consideration of Study Protocols
Emergency (120 day) authorisations
Experimental Permits/Approvals - see Trials Permits
Garden Pesticides: Guidance on Pack Size Limits
Import tolerances and Maximum Residue Levels
The structure of a Notice of Authorisation
Parallel Trade Permit Procedure
Permits for Trials Purposes- see Trials Permits
Reduced water volume: Operator and Efficacy/Crops Safety Risk Assessments
Renewal of Product Authorisations
Withdrawal of Authorisations (Previously revocations of approvals)
Technical specifications and formulation details
The transition from ‘COPR and Directive 91/414/EEC’ to ‘Regulation (EC) 1107/2009’
Transitional arrangements between COPR and PPPR
Trials Permits (previously Experimental Approvals)
Zonal authorisations and mutual recognition under Regulation (EC 1107/2009)
If you have any comments or questions on The Applicant Guide or the associated guidance documents, please contact us at Applicant Enquiries: Link to Contact Details Page.