Applications (new product, amendment and renewal) for PPPs are made in the form of a draft registration report (dRR).
The dRR is split into 3 sections:
- Part A: risk management
- Part B: data evaluation and risk assessment
- Part C: confidential information
Template
Use the template below to create your dRR by downloading and completing each section. Please note that applications for products containing micro-organisms require a different template to be completed.
Part A: Risk management
Summary of Evaluation (.docx) [1]
Part B: Data evaluation and risk assessment
- Section 1, 2 and 4
Identity, Physical and chemical properties and Further information (.docx) [2] - Section 3
Efficacy Data and Information (.docx) [3] - Section 5
Analytical methods Detailed summary of the risk assessment (.docx) [4] - Section 6
Mammalian Toxicology (.docx) [5] - Section 7
Metabolism and Residues (.docx) [6] - Section 8
Environmental Fate Detailed summary of the risk assessment (.docx) [7] - Section 9
Ecotoxicology Detailed summary of the risk assessment (.docx) [8] - Section 10
Assessment of the relevance of metabolites in groundwater (.docx) [9]
Part C: Confidential information
Confidential information (.docx) [10]
Template for micro-organism applications
Part A: Risk management
Summary of Evaluation (.docx) [11]
Part B: Data evaluation and risk assessment
- Section 1
Identity, Physical and chemical properties and Further information (.docx) [12] - Section 2
Analytical methods (.docx) [13] - Section 3
Mammalian Toxicology (.docx) [14] - Section 4
Metabolism and Residues (.docx) [15] - Section 5
Environmental Fate (.docx) [16] - Section 6
Ecotoxicology (.docx) [17] - Section 7
Efficacy Data and Information (.docx) [18]
Part C: Confidential information
Confidential information (.docx) [19]