Data Requirements for Use Site Category (USC # 13): Terrestrial Feed Crops - End Use Products

Data Requirements for Use Site Category (USC # 13): Terrestrial Feed Crops - EP
Data Code Title Data required Conditions Volume No and Pages
0 Index R    
1 Label R    
3 Chemistry Requirements for the Registration of Manufacturing Concentrates and End-Use Products Formulated from Registered technical grade of active ingredients or integrated system products      
3.1 Product Identification      
3.1.1 Applicant's Name and Office Address R    
3.1.2 Formulating Plant's Name and Address R    
3.1.3 Trade Name R    
3.1.4 Other Names R    
3.2 Formulation Process      
3.2.1 Description of Starting Materials R    
3.2.2 Description of the Formulation Process R    
3.2.3 Discussion of the Formation of Impurities of Toxicological Concern CR If applicable  
3.3 Specifications      
3.3.1 Establishing Certified Limits R    
3.3.2 Control Product Specification Form R    
3.4 Product Analysis      
3.4.1 Enforcement Analytical Method R    
3.4.2 Impurities of Toxicological Concern CR If applicable  
3.5 Chemical and Physical Properties      
3.5.1 Colour CR Required for manufacturing concentrates and for EPs which expect to affect product efficacy  
3.5.2 Physical State R    
3.5.3 Odour CR Required for manufacturing concentrates and for EPs which expect to affect product efficacy  
3.5.4 Formulation Type R    
3.5.5 Container Material and Description R    
3.5.6 Density or Specific Gravity R    
3.5.7 pH R    
3.5.8 Oxidizing or Reducing Action (Chemical Incompatibility) R    
3.5.9 Viscosity R    
3.5.10 Storage Stability Data R    
3.5.11 Flammability R    
3.5.12 Explodability R    
3.5.13 Miscibility R    
3.5.14 Corrosion Characteristics R    
3.5.15 Dielectric Breakdown Voltage R    
3.6 Sample(s) CR If requested by PMRA  
3.7 Other Studies/Data/Reports CR If available  
4 Toxicology      
4.1 Summaries R    
4.6 Acute Studies - EP      
4.6.1 Acute Oral R    
4.6.2 Acute Dermal R    
4.6.3 Acute Inhalation R    
4.6.4 Primary Eye Irritation R    
4.6.5 Primary Dermal Irritation R    
4.6.6 Dermal Sensitization R    
4.6.7 Potentiation/Interaction CR If available  
4.6.8 Other Acute Studies CR If available  
4.7 Short-term Studies - EP CR Depending on use pattern, required if any component of the EP may increase absorption of the active ingredient (s) or increase toxic or pharmacologic effects  
4.7.1 Short-term Oral (90-day rodent) CR See 4.7  
4.7.2 Short-term Oral (90-day and/or 12-month dog) CR See 4.7  
4.7.3 Short-term Dermal (90-day) CR See 4.7  
4.7.4 Short-term Dermal (21/28-day) CR See 4.7  
4.7.5 Short-term Inhalation (21/28-day) CR See 4.7  
4.7.6 Short-term Inhalation (90-day) CR See 4.7  
4.7.7 Other Special Studies CR See 4.7  
4.8 Other Studies/Data/Reports CR If available  
5 Exposure (Occupational and/or Bystander)      
5.1 Summaries R    
5.2 Use Description/Scenario (Application and Post Application) R    
5.3 Pesticides Handlers Exposure Database Assessment (or other database) R One of 5.3, 5.4 or 5.5 is required  
5.4 Mixer/Loader/Applicator- Passive Dosimetry Data R See 5.3  
5.5 Mixer/Loader/Applicator-Biological Monitoring Data R See 5.3  
5.6 Post Application - Passive Dosimetry Data CR 5.6 or 5.7 may be required if there is potential for post-application exposure  
5.7 Post Application - Biological Monitoring Data CR See 5.6  
5.8 Dermal Absorption (in vivo) CR Required if margin of exposure is inadequate  
5.9 Dislogeable Residues (Foliar, Soil and Surface) CR Required if there is potential for post-application exposure or to establish re-entry times  
5.11 Glove/Clothing Penetration Data CR May be required for risk mitigation purposes or for inadequate margin of exposure  
5.13 Package Integrity Study CR Required if packaged in water soluble bags  
5.14 Other Studies/Data/Reports CR If available  
6 Metabolism/Toxicokinetics Studies (TGAI or EP)      
6.1 Summaries R    
6.2 Livestock R    
6.3 Plant R    
6.4 Other Studies/Data/Reports CR If available  
7 Food, Feed and Tobacco Residue Studies      
7.1 Summaries R    
7.2 Analytical Methodology (Food Crops & Tobacco)      
7.2.1 Supervised Residue Trial Analytical Methodology R    
7.2.2 Enforcement Analytical Methodology R    
7.2.3 Inter-laboratory Analytical Methodology Validation R    
7.2.4 Multi-residue Analytical Methodology Evaluation R    
7.2.5 Storage Stability of Working Solutions in Analytical Methodology R    
7.3 Freezer Storage Stability Tests CR If stored for more than 30 days and/or volatile or labile study required  
7.4 Crop Residue Data      
7.4.1 Supervised Residue Trial Study R    
7.4.2 Residue Decline Study R    
7.4.3 Confined Crop Rotation Trial Study CR Depends on petitioned uses and cropping practices  
7.4.4 Field Crop Rotation Trial Study CR Depends on cropping practices and/or results from 7.4.3  
7.4.5 Processed Food/Feed CR Depends on on processed commodities and practices  
7.4.6 Residue Data for Crops used as Livestock Feed R    
7.5 Livestock, Poultry, Egg and Milk Residue Data (from feeding of treated crops) R    
7.8 Other Studies/Data/Reports CR If available  
8 Environmental Chemistry and Fate      
8.1 Summaries R    
8.2 Laboratory Studies      
8.2.3 Laboratory Studies of Transformation      
8.2.3.1 Summary R    
8.2.3.6 Special Studies Related to Use-Pattern or Formulation CR    
8.2.4 Laboratory Studies of Mobility      
8.2.4.1 Summary R    
8.2.4.6 Special Studies Related to Use-Pattern or Formulation CR    
8.3 Field Studies of Dissipation/ Accumulation [May be Small or Large-Scale]      
8.3.1 Summary R    
8.3.2 Terrestrial      
8.3.2.1 Canada R    
8.3.2.2 Northern U.S. CR Can substitute for some Canadian studies  
8.3.3 Aquatic      
8.3.3.1 Canada CR Based on potential for aquatic exposure and if pesticide residues have the potential for persistence, mobility, non-target aquatic toxicity or bioaccumulation  
8.3.3.2 Northern U.S. CR Can augment Canadian studies  
8.3.4 Special Studies Related to Intended Use Pattern CR Based on concerns arising from results of other studies  
8.4 Storage, Disposal and Decontamination (TGAI or EP)      
8.4.1 Summary CR    
8.5 Other Environmental Fate Studies (TGAI or EP)      
8.5.1 Summary CR Based on concerns arising from results of other studies  
8.6 Other Studies/Data/Reports CR If available  
9 Environmental Toxicology      
9.1 Summary R    
9.2 Non-Target Terrestrial Invertebrates      
9.2.1 Summaries R    
9.2.8 Laboratory Studies CR If there is a potential for exposure and components of the EP are of concern  
9.2.9 Field Studies CR Based on concerns arising from results of other studies  
9.3 Non-Target Freshwater Invertebrates      
9.3.1 Summary R    
9.3.5 Laboratory Studies CR If components of the EP are of concern  
9.3.6 Field Studies CR Based on concerns arising from results of other studies  
9.4 Non-Target Marine Invertebrates      
9.4.1 Summary CR If there is a potential for estuarine/marine exposure  
9.4.6 Laboratory Studies CR If there is a potential for exposure and components of the EP are of concern  
9.4.7 Field Studies CR Based on concerns arising from results of other studies  
9.5 Fish      
9.5.1 Summaries R    
9.5.4 Laboratory Studies CR If components of the EP are of concern  
9.5.5 Field Studies CR Based on concerns arising from results of other studies  
9.6 Wild Birds      
9.6.1 Summary R For granular formulations, the summary should include: (a) granule size (mm) distribution by weight; (b) number granules/kg product; (c) g ai/kg product; (d) kg product/ha; and (e) type of carrier (e.g., type of clay, corn cob, cellulose, etc)  
9.6.4 Laboratory Studies CR If there is a potential for exposure and components of the EP or the EP itself (e.g., granular formulations) are of concern  
9.6.5 Field Studies CR Based on concerns arising from results of other studies  
9.6.6 Special Studies Related to the Intended Use-Pattern (TGAI and EP) CR See 9.6.5  
9.7 Wild Mammals      
9.7.1 Summary CR Based on concerns arising from results of other studies  
9.7.2 Field Studies CR See 9.7.1  
9.8 Non-Target Plants      
9.8.1 Summary R    
9.8.6 Laboratory Studies CR If components of the EP are of concern  
9.8.7 Field Studies CR Based on concerns arising from results of other studies  
9.9 Other Studies/Data/Reports CR If available  
10 Value (applicable to each pest/site or host combination)      
10.1 Value Summaries R    
10.2 Efficacy Studies      
10.2.1 Mode of Action R    
10.2.2 Description of Pest Problem R    
10.2.3 Efficacy Trials      
10.2.3.1 Summaries R    
10.2.3.2 Efficacy: Laboratory, Growth Chamber Trials CR One or both of 10.2.3.2 or 10.2.3.4 may be required  
10.2.3.3 Efficacy: Small-scale Trials (Field, Greenhouse) R    
10.2.3.4 Efficacy: Operational Trials CR See 10.2.3.2  
10.3 Adverse Effects on Use Site      
10.3.1 Summaries R    
10.3.2 Non-Safety Adverse Effects [e.g.: to crop, site of application (discoloration, corrosion), etc.] R    
10.3.3 Damage to Rotational Crops CR    
10.4 Economics CR    
10.5 Sustainability      
10.5.1 Survey of Alternatives (chemical and non-chemical) CR    
10.5.2 Compatibility with Current Management Practicesn Including IPM CR    
10.5.3 Resistance Management CR    
10.5.4 Contribution to Risk Reduction CR    
10.6 Other Studies/Data/Reports CR If available  
12.5 Foreign Reviews      
12.5.3 Foreign Reviews of Chemistry Requirements for MAs and EPs formulated from registered TGAIs or ISPs CR    
12.5.4 Foreign Reviews of Toxicology CR    
12.5.5 Foreign Reviews of Exposure (Occupational and/or Bystander) CR    
12.5.6 Foreign Reviews of Metabolism / Toxicokinetics Studies CR    
12.5.7 Foreign Reviews of Food, Feed and Tobacco Residue Studies CR    
12.5.8 Foreign Reviews of Environmental Chemistry and Fate CR    
12.5.9 Foreign Reviews of Environmental Toxicology CR    
12.5.10 Foreign Reviews of Value CR    
12.7 Comprehensive Data Summaries R    
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