T-4-113 (Suppl.1) - Data Requirements for Product Safety Evaluations: Explanatory Notes
This guideline provides an explanation of the data requirements for safety evaluations of fertilizers and soil supplements. It is to be used in conjunction with Trade Memorandum T-4-113 - Guidelines to Safety Assessments of Fertilizers and Supplements and to Information to be Submitted in Demonstrating Product Safety.
Table of Contents
- Name and Synonyms
- Use Patterns
- Species of Intended Use
- Unit Amount
- Product Label
- Material Safety Data Sheet (MSDS) for Product or Ingredients
- Outline of Manufacture
- Name and Synonyms
- Chemical Abstract Service Number
- Chemical Formula (Molecular and Structural)
- Concentrations in the Finished Product
- Criteria for Chemical Identity and Purity
- Estimated Shelf Life
- Molecular Weight
- Physical State
- Particle Size
- Colour and Odour
- Olfactory Detection Limit
- Density/Specific Gravity
- Refractive Index
- Melting Point
- Boiling Point
- Flash Point
- Auto-Ignition Point
- Vapour Pressure
- Vapour Density
- Henry's Law Constant
- Octanol-Water Partition Coefficient
- Dissociation Constant
- Rate and Degree of Absorption
- Distribution, Metabolism and Excretion Data
- Acute Toxicity
- Acute Median Lethality
- Skin/Eye Irritation
- Skin Sensitization
- Short-Term Toxicity
- Developmental Toxicity
- Reproductive Toxicity
- Epidemiological Studies
- Chemical Interaction
- Major Routes of Exposure
- Amount of Product Handled by Workers and Consumers
- Frequency and Duration of Exposure
- Exposure Concentrations
- Exposure Studies
- Crop Identification
- Rates, Timing Intervals to Harvest
- Plant Metabolism Data
- Product, Metabolite and/or Contaminant Residue Studies
- Analytical Methods for Metabolism and Residue Studies
- Metabolic Fate Studies
- Residue Studies for the Parent Compound and its Possible Metabolites
- Excretion Data
- Vapour Pressure and Volatilization
- Dissociation Constant
- Solubility in Water
- Henry's Law Constant
- Octanol-Water Partition Coefficient
- Biotransformation in Soil
- Biotransformation in Aquatic Systems
- Biochemical Oxygen Demand
- Toxicity to Aquatic Organisms
- Toxicity to Soil Organisms
- Toxicity to Birds and Mammals
- Toxicity to Wildlife
1. Identification and Use of the Product
a. Name and Synonyms:
The name of the product as it appears on the product label or shipping bill.
Commonly used alternates or acronyms, including names used in other countries, most common chemical name, a botanical or species identification, etc.
b. Use Patterns
This describes the intended use of the product. The type of information required includes:
- mixing information if used in conjunction with other products;
- suggested rates of application;
- times, frequency and methods of application;
- recommended safety measures;
- distribution, storage, and handling information;
- recommended emergency measures;
- strategies for re-use, resale or disposal of unused product.
The Use Pattern should clearly specify whether the product will be used in food production and whether it will be used indoors or outdoors, contained or uncontained, etc.
c. Species of Intended Use
Identify all plant species and soil types for which the product is intended (if not described under Use patterns).
d. Unit Amount
How and in what quantities is the product to be sold, transported and stored? (i.e., 50 L metal drum, 20 kg plastic-lined canvas sack, etc.)
e. Product Label
A copy of the product label (if applicable) or bill of lading conforming to the appropriate Regulations must be provided.
f. Material Safety Data Sheet (MSDS) for Product and Ingredients
An MSDS is a comprehensive technical bulletin containing detailed information on a substance or product. It is a basic source of information for preliminary safety evaluations identifying points (such as possible contaminants) which may need to be examined in greater detail. An MSDS should also provide a detailed explanation of precautions and protective measures. The Workplace Hazardous Materials Information System (WHMIS) provides criteria for developing an MSDS.
g. Outline of Manufacture
A general description of the production and formulation processes, identifying raw materials, chemical reactions, techniques and any other parameters which may influence the specifications, hence quality or safety of a product. This will serve as background information relating to product purity and any recycled materials (e.g., by-products and wastes) used in manufacturing or formulating the end-product.
A flow-chart diagram accompanying the description is preferred.
2. Chemical Components Including Impurities
a. Name and Synonyms
The exact chemical name and synonyms of all ingredients, including significant contaminants or impurities should be listed. For substances which need to be described by the reaction producing them (UVCBs), see CEPA Guidelines, section 4, and Appendix III.
b. Chemical Abstract Service Number (CAS No)
An identification number is assigned by the Chemical Abstracts Service (CAS) to differentiate between known chemicals. This is a useful reference when searching for technical information and should be provided for each ingredient.
c. Chemical Formula (Molecular and Structural)
The molecular formula identifies the basic elements (atoms) of molecules. A structural formula is a diagram of the bonds between atoms. Comparing these with the formulae of substances whose properties are known is useful in anticipating hazards of substances which have not themselves been tested. Where isomeric mixtures exist, (closely related chemical variants), the ratio of isomers should be included, since this may affect toxicity. For polymers, (long chains of molecules), the structural formulae should show the repeating unit(s), along with an identification of links and cross-links.
d. Concentrations in the Finished Product
The amount of all ingredients in the commercial product should be expressed as a percent by weight or by parts per million (ppm).
e. Criteria for Chemical Identity and Purity
The exact formulation of a particular product may vary, depending upon the manufacturer. A precise description of ingredients including contaminants is needed to properly assess product safety (for example, a nuclear magnetic resonance (NMR) spectrum, or a gas chromatography (GC) profile).
f. Estimated Shelf Life
This is the length of time the product can be stored without alterations to its chemical/biological integrity. This includes not only times under ideal conditions, but a description of the factors affecting shelf life, what happens when the product degrades or decays, how one can tell, whether this creates a particular hazard, and how the manufacturer has substantiated its estimation of shelf life.
3. Method(s) of Analysis, Recovery, and Detection Iimit Data for the Analyses
An acceptable test method for the analysis of the proposed product must be provided. This method must establish statistically relevant recovery and detection limits and must allow third-party technicians to identify and quantify the active ingredients. For specific requirements of analytical methods, please see Good Laboratory Practices Protocol for Fertilizer and Supplement Registration.
4. Physicochemical Data
Physicochemical data is used to identify and differentiate between substances or products and to assist in predicting or determining the behaviour of substances in the human body, other organisms or the environment. Please note the reference protocols associated with each data point. Unless otherwise specified, these data points apply to the technical grade formulation of the substance and not to an analytically purified sample.
a. Molecular weight
Every chemical has a characteristic molecular "weight" determined by the elements or atoms that make it up. In the case of polymers, (molecules composed of atomic "chains" of varying length), an average is given to describe molecular weight and testing is performed on the lowest number-average composition.
b. Physical state
This indicates whether a substance or product is solid, liquid or gaseous at room temperature.
This describes the form of the product, such as a granular solid, gelatinous liquid, or a fine powder.
d. Particle Size
If the substance is solid, what is its average particle size? What is the range of particle sizes, and their proportion of distribution? This property may be a significant factor determining the distribution and uptake of a substance, for example, whether it is taken up by organisms or inhaled into human lungs.
e. Colour and Odour
Include this description for the chemical ingredients as well as for the formulated product, including any noted variations.
f. Olfactory Detection Limit
This is the minimum concentration (e.g., parts per million by volume in air), at which one can identify the substance by smell. This is important in determining whether or not smell can serve as an appropriate warning of the presence of the substance.
g. Density/Specific Gravity
For solids, this is measured as mass per volume (i.e., g/mL). For liquids, specific gravity compares density to that of water, which is assigned a value of 1 (i.e., 2.0 is twice as dense as water, 0.50 is half as dense). These measurements are used in several ways, such as when predicting the behaviour of a substance in the environment.
h. Refractive Index
The speed of light changes as light passes from one medium to another, causing it to "bend," (as objects partially inserted into water look bent.) This property varies from one substance to another and is sometimes useful in identifying substances using a simple, accurate technique.
i. Melting Point
The temperature, at a specified pressure, at which a solid becomes liquid. Some chemicals break down or undergo chemical reaction before reaching their melting point; details of this should be identified.
j. Boiling Point
The temperature, at a specified pressure, at which a liquid becomes a gas. Some chemicals break down or undergo chemical reaction before reaching their boiling point; details of this should be identified.
k. Flash Point
The minimum temperature at which a liquid gives off enough flammable vapours that these will ignite on contact with a flame or spark. This has obvious implications for worker safety during handling and storage.
l. Auto-Ignition Point
The minimum temperature at which a flammable liquid will ignite spontaneously without an ignition source. Again, an important safety parameter.
m. Vapour Pressure
This is a measure of a liquid's ability to evaporate, or give off vapours at specific temperatures. Usually expressed in millimetres of mercury (mmHg), it is a crucial indicator of the behaviour of a liquid product, indicating, for example, whether it will tend to escape to the atmosphere or remain in soil.
n. Vapour Density
A comparison between the mass of a gas and that of dry air which is assigned a value of 1, (i.e., 2.0 is twice as dense as air, 0.50 is half as dense). This is another important indicator of how a substance will behave. Less dense gases tend to rise and are quickly transported throughout the environment; heavier gases remain closer to the ground and dissipate less rapidly.
o. Henry's Law Constant
This is a measure of the solubility of a gas in liquid. It is indicative of a substance's tendency to move from water to air or vice-versa.
Indicates if a substance is acidic, alkaline or neutral and how strong an acid or base it is. Besides measuring potential corrosivity, pH can have a major effect on the interactions of a substance with living organisms, such as the degree to which it is absorbed or taken up.
- in Water: This measures the amount of a substance that will dissolve in water at a given temperature. Since water supports life and since many chemicals dissolve in water to a significant degree, it is often the route by which chemicals are taken up by organisms. It is also used in predictions of environmental fate of substances.
- in Other Solvents: This measures the amount of a substance that will dissolve in solvents other than water. This provides a guide for choosing a solvent to extract a chemical from organic tissue or soil for further analysis, for instance.
r. Octanol-Water Partition Coefficient
This measures the tendency of a substance to separate, either into organic solvents or into water. A fundamental toxicological data point, it is used in predicting whether a substance may build up in the fatty tissues of an organism and in predicting its tendency to adhere to soil particles.
s. Dissociation Constant
Dissociation is a specific type of chemical decomposition in which a molecule breaks up into charged particles called ions. Ions, in turn, are often involved in further chemical reactions and may be absorbed or distributed at a different rate. For given conditions, the rate of dissociation expressed as a value (the dissociation constant) is constant.
Some substances react violently or explosively with other substances. If the formulated product or any of its ingredients should not come in contact with certain substances, this must be reported.
Some substances may spontaneously polymerize (form long molecular chains) under certain conditions. Many of these reactions give off dangerous or explosive amounts of heat. Any such substances contained in the formulated product must be identified along with a description of conditions under which spontaneous polymerization is known to occur.
5. Mammalian Toxicological Data
In order to assess the potentially harmful effects of substances on mammals, information from laboratory-scale tests is necessary. The type of toxicity data generally considered is outlined below.
a. Rate and Degree of Absorption
For each route by which a substance can be taken into the body (oral, dermal, respiratory, etc.), absorption tests determine how extensively and how rapidly it can be absorbed.
b. Distribution, Metabolism and Elimination Data
These tests describe the fate of a chemical once it is absorbed into the body. Where does it go? Does it accumulate? How is it broken down or transformed? By what route and how quickly is it eliminated? This information provides an indication of an organism's ability to tolerate short or long-term exposure, either at high or low concentrations. It is useful information in designing toxicity tests, e.g., in dose selection. It also aids in extrapolating animal data to human conditions.
c. Acute Toxicity
Acute exposure tests examine the effects of short-term, single exposures to high concentrations of a substance. Exposures in these tests are typically 24 hours or less, with effects being monitored for two weeks. This is the first step in establishing the toxic potential of substances. This is especially useful for establishing the crucial relationship between the dose and the response, for ranking substances according to their relative acute toxicity and for classification and precautionary label statements. Acute toxicity data is used to obtain preliminary information on specific toxic effects of substances and how these may be produced (mode of action). Some specialized acute tests are described below.
- Acute Median Lethality:
The concentration of a substance which, when administered once to a group of animals for a short time, will cause death in half of the animals. This is expressed as an LD50, (lethal dose, in mg/kg of body weight), or LC50, (lethal concentration, in parts per million).
- Skin/Eye Irritation:
This determines if a substance has the potential to cause irritation or cell death (necrosis) when in contact with the skin or eyes.
- Skin Sensitization:
Property of being able to "sensitize" organisms: Organisms may become more sensitive to a substance after an initial exposure and develop allergic reactions in subsequent exposures.
A screening test in determining a substance's potential for causing genetic mutations which may lead to cancer or malformations in offspring. At least two types of tests are performed, conventionally one with bacteria and one with mammalian cell cultures. It is also necessary to perform tests with and without "activation," that is, to determine if interaction with metabolic processes in the body makes a substance "mutagenic".
e. Short-Term Toxicity
Short-term toxicity studies involve repeated exposure to substances over a longer (more typical) time frame. They are useful for detecting most longer-term adverse health effects, for establishing a threshold level at which no-observed-effect level (NOEL), for establishing possible cumulative effects of exposure, species and other types of variation and for suggesting appropriate conditions for chronic tests, if deemed necessary. A 90-day oral study is typical, but inhalation and dermal studies may be more appropriate, depending on typical human exposure conditions.
These types of tests explore the possibility of birth defects resulting from parental or placental exposure to chemicals.
g. Developmental Toxicity
These tests examine adverse effects during the lifetime of an organism prior to conception, during pre-natal development or until puberty, resulting from exposure of either parent to a substance.
h. Reproductive Toxicity
Adverse effects of substances on male or female reproductive systems and capacity (from mating through lactation).
Where indicated by earlier tests or other data, a substance will be examined for its ability to induce cancer (tumours) in animals. Tests are typically conducted over a major portion of the animal's life span, often combined with chronic toxicity tests.
j. Epidemiological Studies
This type of study contains a compilation and analysis of information on humans who have been occupationally or accidentally exposed to a substance.
k. Chemical Interaction
The toxic effect of a substance can sometimes be altered, either increased, decreased, or changed entirely by interactions with other substances. A toxin may be rendered harmless by another, or its effect may be magnified many times. Data to identify and measure the significance of such interactions improves the hazard assessment for the substance.
6. Suggested Maximum Residue Limit (mrl) or Tolerance
An MRL is to be suggested, based on an evaluation of information, such as mammalian toxicity data, dietary intake estimates and livestock metabolism data.
This criteria governs the concentration of a chemical that may build up in the tissues of plants or livestock without causing harm to the plant or animal, or to the humans that consume their products.
7. Human Exposure Data and Exposure Estimation
The following information is important in assessing the degree of exposure of workers and users to particular substances.
a. Major Routes of Exposure
Human exposure to a substance depends, in part, on how it can be taken up by the body, whether via the respiratory route, skin absorption, oral ingestion, etc. Based on the properties of a product's ingredients, its formulation and methods of use, how might users be exposed?
b. Amount of Product Handled by Workers and Consumers
What is the total quantity of product that would typically be used in a given application cycle (e.g., 50 litres/day)?
c. Frequency and Duration of Exposure
How often and how many times will the product normally be used? How long is the product used each time?
d. Exposure Concentrations
How concentrated is the product when transported, stored and actually used? Is it diluted before use? Include references to intermediate preparation steps, such as mixing.
e. Exposure Studies
Include all data on human exposure, uptake into the body, and medical studies of workers who have been exposed to the product over long periods of time. In some cases exposure studies may have to be conducted to establish how much absorption into and distribution through the body takes place with intended conditions of use.
8. Specifics for Food Plant Usage
The following information is required to assess the safety of substances to be used in conjunction with food crops.
a. Crop Identification
This indicates the specific agricultural crop(s) on which the product is intended to be used.
b. Rates, Timing, Intervals to Harvest
This section is to specify exactly how a product will be used and applied, including the rates of application, times at which the product is to be used and the intervals between application and harvest. These are important in determining whether it or its break-down products will remain in a crop at the time of harvest or when consumed by humans. This information is required for each crop.
c. Plant Metabolism Data
This information describes the fate of a substance in the plant; how it is broken down; what is the break-down product; to what extent does it break down; and at what rate. This study should include the levels and identities of the resulting breakdown products.
d. Product, Metabolite and/or Contaminant Residue Studies
These tests determine the amount of parent substances, contaminants or their break-down products which remain as residues in a particular crop at harvest or when consumed. This is a most important step in establishing the potential exposure of humans through the food chain. Residue studies are performed using recommended crops and rates, timing, and intervals of harvest.
It is possible that one characteristic, such as germination, be improved at the expense of another, such as yield. Plant toxicity or phytotoxicity tests investigate these possibilities.
f. Analytical Methods for Metabolism and Residue Studies
The submitted data must be accompanied by a description of the analytical methods upon which it is based. This will enable us to evaluate the accuracy and usefulness of the data. Recovery and detection limits should be included.
9. Livestock Metabolic Fate and Residue Studies
Mammalian toxicity data derived from tests on mice and rats offer limited information on the risk of a particular substance to several livestock species. The following data requirements involve direct testing with livestock and apply to products the livestock are likely to be exposed to via their feed.
a. Metabolic Fate Studies
These tests describe exactly what happens to a substance once it is ingested by livestock. How is it absorbed, and how quickly? How is it distributed throughout the body and how quickly? How is it broken down, and what are the resultant metabolites (by-products)? By what route is the substance and its metabolites eliminated from the body, and at what rate? What is their "half-life?". Appropriate methods for the recovery and analysis of the substance and its metabolites in animal tissues should be included. Detection limits of such methods must be stated.
b. Residue Studies for the Parent Compound and its Possible Metabolites
Residues in livestock tissue have the potential to enter the human food chain. Thus, it is important to determine how much of a substance actually remains in exposed animals and in which tissues it occurs. This data requirement should also include statistically significant analytical techniques for recovery and detection limits in animal tissues.
c. Elimination Data
The ability of an organism to break down and eliminate a substance is a major consideration in evaluating the hazards of a substance. Elimination data provides a quantitative determination of this ability and indicates how effectively livestock can deplete a chemical.
10. Environmental Fate and Effects
The following data requirements, in combination with the physicochemical data, form the basis for predicting or determining which parts of the environment will be "exposed" to a substance following its release (or the release of its break-down products) and how the organisms therein may be affected.
a. Vapour Pressure and Volatilization
This is a measure of a liquid's ability to evaporate or give off vapours at specific temperatures. Usually expressed in millimetres of mercury (mmHg), it is a crucial indicator of the behaviour of a liquid product, for example, whether it will escape to the atmosphere or remain in soil.
b. Dissociation Constant
Dissociation is a specific type of chemical decomposition in which a molecule breaks up into charged particles called ions. Ions, in turn are often involved in further chemical reactions and may be absorbed or distributed at a different rate. For given conditions, the rate of dissociation expressed as a value (the dissociation constant) is constant. This can indicate how reactive the chemical may be.
One of the main ways in which substances break down in the environment is by splitting through combination with water molecules. The extent to which this reaction may take place under normal conditions and the by-products of this type of reaction should be described.
Another important way in which substances are broken down is by interaction with light. Tests are used to determine the potential for such degradation as well as the substance's break-down products following this type of reaction.
e. Solubility in Water
This measures the amount of a substance that will dissolve in water at a given temperature. Since water supports life and since many chemicals dissolve in water to a significant degree, it is often the route by which chemicals are taken up by organisms. It is also used in predictions of environmental fate of substances.
f. Henry's Law Constant
This is a measure of the solubility of a gas in liquid. It is indicative of a substance's tendency to move from water to air or vice-versa.
g. Octanol-Water Partition Coefficient
This measures the tendency of a substance to separate, either into organic solvents or into water. A fundamental toxicological data point, it is used in predicting whether a substance may build up in the fatty tissues of an organism, and in predicting its tendency to adhere to soil particles.
The ability of a substance to adsorb or become "attached" to and then desorb or detach from other particles or molecules, such as soil, affects how quickly it may move through, or how long it may remain in a particular environment.
This type of study establishes the potential for substances to move through different types of soil, usually under the influence of water movement. This helps to predict whether land-applied substances will reach ground water.
j. Biotransformation in Soil
Some substances undergo changes as a result of transformation by microorganisms, i.e., "biodegradation". These tests determine the potential for biodegradation and the break-down products which result from biodegradation. Data for both aerobic and anaerobic conditions (in the presence or absence of oxygen) are useful because different microorganisms are involved in each case and both conditions are found in the environment.
k. Biotransformation in Aquatic Systems
As with soil biotransformation, substances may be transformed by the microbial reactions in an aquatic environment. Data for aerobic and anaerobic conditions should again be supplied.
l. Biochemical Oxygen Demand
The quantity of oxygen required by microorganisms to oxidize organic compounds in a water sample. Results are measured in mg of oxygen per litre or per gram of compound. Organic contaminants can impair water quality by reducing oxygen levels which in turn adversely affects aquatic organisms.
m. Toxicity to Aquatic Organisms
It is important to establish the adverse effects of substances on aquatic organisms. Often, the mechanisms of these effects are unique to aquatic environments and toxicity cannot be predicted using laboratory mammals. Also, the repercussions of disturbing organisms toward the bottom of the food chain can be very serious to the entire ecosystem.
n. Toxicity to Soil Organisms
The adverse effects of substances on soil organisms is important because the long-term health of agricultural soils can be compromised by disturbing their populations.
o. Toxicity to Birds
The adverse effect of substances on birds can be important.
Birds may be more susceptible to the adverse effects of chemicals than laboratory animals. This difference in tolerance is partly due to differing environmental stresses and conditions as well as to metabolic and behavioral differences between organisms.
p. Toxicity to Wildlife
These toxicity tests are valuable for indicating the adverse effects a chemical will have on animals under actual environmental conditions.
11. Bibliography of Protocols, Test Guidelines, Reference Materials and Services
American Association of Cereal Chemists
- Approved Methods of the American Association of Cereal Chemists, AACC, St Paul, Minnesota: Revised 1982
American College of Veterinary Toxicologists
- Analytical Toxicology Manual
- American College of Veterinary Toxicologists, Kansas State University, Manhattan, Kansas: 1981
Agriculture and Agri-Food Canada (AAFC)
- Guidelines for Developing a Pesticide Toxicology Data Base, Trade Memorandum T-1-245, Agriculture and Agri-Food Canada, 1984
- Good Laboratory Practices Protocol for Fertilizer and Supplement Registrations
Association of Official Analytical Chemists
- Test Protocols for Environmental Fate & Movement of Toxicants, Association of Official Analytical Chemists, Washington, DC: 1980
Amdur, MO et al (editors)
- Casarett and Doull's Toxicology, Fourth edition, Pergamon Press; New York: 1991
American Society for Testing and Materials
- Annual Book of ASTM Standards, (Section 11: Water and Environmental Technology)
Blalock, CR et al (editors)
- Acceptable Common Names and Chemical Names for the Ingredient Statement on Pesticide Labels, (OPP/EPA 1979)
Canadian Environmental Protection Act
- Guidelines for the Notification and Testing of New Substances pursuant to the New Substances Notification Regulations of the Canadian Environmental Protection Act: Chemicals and Polymers, Ottawa, July 23, 1992
Chemical Evaluation Search and Retrieval System (CESARS)
- Michigan Dept of Natural Resources, and Ontario Ministry of the Environment, 1992
- The Shelf Life of Foods and Beverages, Elsevier Science Publishers, Amsterdam: 1986
Chemical Abstracts Service
- 2540 Olentangy River Road, Box 3012, Columbus, Ohio, 43210, Telephone, 614-447-3600 or 800-848-6538
Clesceri, Lenore S, et al (editors)
- Standard Methods for the Examination of Water and Wastewater, seventeenth edition; AWWA, APHA, WPCF; Washington, DC: 1989 (Esp part 8000: Toxicity Test Methods for Aquatic Organisms)
- Analytical Methods Manual, Inland Waters Directorate: Analytical Methods Manual, 1979-1986.
- "Enviroguide" : Série de la Protection de l'environnement, Méthods de référence SPE 1/RM/1 - SPE 1/RM/22 (1992)
Food and Agriculture Organization (FAO)
- See World Health Organization/Food and Agriculture Ogranization (WHO/FAO)
Fazio, T (editor)
- Food Additives Analytical Manual, Volume II: A Collection of Analytical Methods for Selected Food Additives; UsFDA, AOAC, Arlington, Virginia: 1987
Freed, VH, et al
- Some Physical Factors in Toxicological Assessment Tests; in Environmental Health Perspectives 30:75-80 (1979)
- The Assessment of Mutagenicity (1992) The Use of Genotoxicity Tests in Regulation (1989)
- Genotoxicity Assays Recommended in the Health Protection Branch Genotoxicity Committee Report: Conduct and Reporting for Effective Evaluation (1989)
- Compendium of Analytical Methods, Volume 1: Official Methods of Microbiological Analysis of Food; Polyscience Publications and Supply and Services Canada; Ottawa: 1989
- Guidelines on the Use of Mutagenicity Tests in the Toxicological Evaluation of Chemicals, Health Canada, 1986
- Analytical Methods for Residues of Veterinary Drugs, In Rico, AG (ed) Drug Residues in Animals, Academic Press, Incorporated, Orlando, Florida: 1986
Helrich, Kenneth, (editor)
- Official Methods of Analysis of the American Association of Official Analytical Chemists, (15th edition, 1990)
Keith, LH (editor)
- Sampling and Analysis Methods, Compilation of EPA Methods, Lewish Publishers, New York: 1992
Lawrence, James F
- Analytical Methods for Pesticides and Plant Growth Regulators, New York: Academic Press 1972-1989
Lude, David R (editor)
- CRC Handbook of Chemistry and Physics, 72nd edition, 1991-92, Boston: CRC Press
Nair, GE (editor)
- CIPAC Handbook, volumes 1A and 1B; Collaborative, International Pesticides Analytical Council, 1980
National Academy of Sciences
- Testing for effects of chemicals on ecosystems, NRC, National Academy Press: Washington, DC
National Institute of Standards and Technology (NIST)
- Chemical Science and Technology Telephone: 301-975-3145
National Institute for Occupational Safety and Health (NIOSH)
- Manual of Analytical Methods, National Institute for Occupational Safety and Health (NIOSH), Washington, DC: Superintendent of Documents, 198-, volume 6
Official Journal of the European Communities (OJEC)
- Council Directive of 16 February 1987 fixing guidelines for the assessment of additives in animal nutrition, Official Journal of the European Communities, OJ NO L 64/19, II (87/153/EEC)
Ontario Ministry of the Environment
- Handbook of Analytical Methods, Toronto, Ontario: Queen's Printer, 1985
Organization for Economic Co-operation and Development
- OECD Test Guidelines
Paget and Thomson, (editors)
- Standard Operating Procedures in Toxicology Inveresk Research Int'l, Limited; University Park Press, Baltimore: 1979
Stahr, HM (editor)
Analytical toxicology Methods Manual, Supplement; Iowa State University Press, Ames, Iowa: 1980
- Analytical Methods in Toxicology, John Wiley and Sons, Incorporated; New York: 1991
United States Code of Federal Regulations
- Title 40, parts 796, 796, 798: Toxic Substances Control Act Test Guidelines; Final Rules, (1985 and updates)
United States Department of Health and Human Services
- Specifications for the Conduct of Studies to Evaluate the Toxic and Carcinogenic Potential of Chemical, Biological and Physical Agents in Laboratory Animals for the National Toxicology Program (NTP)
United States Environmental Protection Agency
- Pesticide Assessment Guidelines (EPA PAG) Subdivisions D,E,F,G,I,J,K,L,M,N,O and U
- Health Effects Test Guidelines
- Short-term Tests for Health and Ecological Effects
- Test Guidelines: Chemical Fate
- Test Guidelines: Environmental Effects
- New and Revised Chemical Fate Test Guidelines
- New Environmental Effects Test Guidelines
- New and Revised Health Effects Test Guidelines
- Selected Analytical Methods Approved and Cited by the United States Environmental Protection Agency, American Public Health Association, 15th edition, 1981; supplement to Standard Methods for the Examination of Water and Wastewater, 15th edition
- Environmental Protection Agency (EPA)
- Toxicology Handbook Standard Evaluation Procedure: Product Chemistry (1988)
United States Food and Drug Administration
- TOXICOLOGICAL PRINCIPLES for the Safety Assessment of Direct Food Additives and Colour Additives Used in Food United States Food and Drug Administration, Bureau of Foods, 1982
- General Principles for Evaluating the Safety of Compounds Used in Food-Producing Animals, United Stated Department of Health and Human Services, 1986
- Macroanalytical Procedures Manual, FDA Technical Bulletin #5, 1984
- Animal Drug Analytical Manual, United States Department of Health and Human Services, Centre for Veterinary Medicine; AOAC Arlington, VA: 1985
- Pesticide Analytical Manual, Volume 1: Foods and Feeds; United States Food and Drug Administration, Washington, DC: 1987
Wernimont, Grant T
- Use of Statistics to Develop and Evaluate Analytical Methods, Association of Official Analytical Chemists; Virginia: 1985
World Health Organization/Food and Agriculture Organization (WHO/FAO)
- Guidelines for the Study of Dietary Intakes of Chemical Contaminants, WHO Offset Publication no. 87, World Health Organization, Geneva: 1985
- Guide to Short-term Tests for Detecting Mutagenic and Carcinogenic Chemicals, International Program on Chemical Safety, Environmental Health Criteria 51, NEP, ILO, WHO; World Health Organization, Geneva: 1985
- Principles for the Toxicological Assessment of Pesticide Residues in Food, International Program on Chemical Safety, Environmental Health Criteria 104, World Health Organization, Geneva: 1990 Guidelines to CODEX: Recommendations Concerning Pesticide Residues, Part 5; "Recommended Method of Sampling for the Determination of Pesticide Residues"; World Health Organization, Food and Agriculture Organization of the United Nations, Rome: Document number CAC/PR 5-1984, updated at 20th CCPR, 1988
- Guide to specifications for general notices, general analytical techniques, identification tests, test solutions, and other reference materials, Food and Agriculture Organization of the United Nations/World Health Organization, Rome: 1991
- Date modified: