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
- Adjuvants
- Adverse data - Approval Holder Responsibilities
- Application fees
- Application overview
- Applications for addition of undersown crops to product labels
- Application types
- Application - what to include
- Biopesticides
- Classification and labelling requirement on authorisations
- Commercial withdrawals
- Comparative Assessment
- Consideration of study protocols
- Data submission deadlines
- Emergency (120 day) authorisations
- Experimental permits/approvals
- Extensions of use Contents
- Garden pesticides: guidance on Pack size limits
- Import tolerances and Maximum Residue Levels (MRLs)
- Letters of access
- Notice of Authorisation structure
- Northern Ireland only Parallel Trade Permit Procedure
- Permits for trials purposes
- Procedures for submission and assessment of confirmatory data following inclusion of an active substance in Annex I of Council Directive 91/414/EEC
- Protection of data
- Product registration numbers
- Reduced water volume: operator and efficacy/crops safety risk assessments
- Renewal of product authorisations
- Withdrawal of Authorisations (Previously revocations of approvals)
- Streams and targets
- Tank-mixes
- 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)
- Two-stage applications
- 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.