The Applicant Guide: Guidance
The Applicant Guide explains how to submit an application to HSE, how we process the application, what should be included and what happens once the application is completed.
In addition to the Guide, guidance to address different aspects of plant protection product (PPP) and adjuvant registration is available. Links to these documents can be found in the appropriate places in The Applicant Guide but a list of these documents is detailed below.
The Applicant Guide associated Guidance
Active substance approval – The decision- making process
New active substance 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
Consideration of study protocols
Emergency (120 day) authorisations
Experimental permits/approvals
Garden pesticides: guidance on Pack size limits
Import tolerances and Maximum Residue Levels (MRLs)
Notice of Authorisation structure
Northern Ireland only Parallel Trade Permit Procedure
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
Implications of active substance renewal for ongoing applications, new applications and existing authorised products (transitional arrangements during the frozen period)
Trials Permits (previously experimental approvals)
Authorisation under Article 40 of Regulation 1107/2009 (NI)
If you have any comments or questions on The Applicant Guide or the associated guidance, please contact us at Applicant Enquiries.