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The first is the probability of an adverse health effect, ie what is the likelihood that there will be microbiological contamination of a food stuff? The second component is the severity of the effect; for example there may be a high likelihood of some amount of microbiological contamination of a food, but at the levels at which it occurs it may not affect the health of people very much. Conversely, you may have a situation in which the probability of having a pathogen present in food is very low, but if it is present, it will have a severe effect on the health of people eating the food. You will have to decide if will treat these situations differently.F   u  ^ H  0޽h ? ̙330 phP8(  8d 8 c $!   \ 8 3 rT\oj7oj7 >   \I would like to use the remainder of my time today to talk about how WHO works with risk managers like Codex in a process called risk analysis. Risk analysis is a process composed of three parts: Risk management, risk assessment, and risk communication. Risk assessment is the scientific evaluation of known or potential adverse health effects resulting from human exposure to foodborne hazards. WHO together with FAO conduct scientific evaluations of known or potential adverse health effects resulting from human exposure to foodborne hazards. Risk communication is an interactive process of exchange of information and opinion on risk among risk assessors, risk managers, and other interested parties. Risk management is the process of weighting policy alternatives in the light of the results of risk assessment and, if required, selecting and implementing appropriate control options, including regulatory measures. An international risk manager for the protection of public health from foodborne illness already exists. The Codex Alimentarius Commission establishes international policy for food safety. ]]] H 8 0޽h ? ̙33 0 X4(  Xd X c $    X s *$ @   These four steps are not sequential; the results from the hazard characterisation and the exposure assessment must to be drawn together to give some indication of the risk; sometimes this is called the risk estimate.*A   H X 0޽h ? ̙33 0 |Pd(  dd d c $   p d s * @   The process of weighing policy alternatives in the light of the results of the risk assessment and, if required, selecting and implementing appropriate control measures, including regulatory measures. The risk management measure that is implemented will very much depend on the level of food safety that the community demands,ie the level of risk that the community is prepared to accept. In some senses knowledge of the community comes from past history or perhaps more recent statements by governments. The policy parameters that might be considered include: The level of risk that the community is willing to accept The severity and frequency of the the adverse health effect Community  outrage International obligations (WTO) Government regulatory policy  minimum effective regulation Enforceability Feasibility Cost/benefit (6E*I   H d 0޽h ? ̙33 0 (  d c $   v s *1 @   4Chemical hazards: egs residues, additives/processing aids, environmental contaminants, toxins. Hazard identification establishes the toxicity of a substance; for example, by structural and associated physiochemical properties, metabolism and toxicokinetics, toxicity testing in animal models and /or in vitro testing. Microbiological hazards: Identify organisms or microbial toxins. The International Union for Microbiological Specifications has categorised the most serious and common hazards according to severity. Data on microbiological hazards also comes from controlled human studies, epidemiological studies and studies of outbreaks of foodborne disease. 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