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ANNEX IV - USE OF ELEMENTS OF (QUANTITATIVE) MICROBIOLOGICAL RISK ASSESSMENT BY INDUSTRY


Industry has the responsibility for producing safe foods. Industrial Food Safety Management includes various general quality assurance systems, particularly HACCP and its prerequisite systems (GMP, GHP), and optimization of hazard control throughout the food supply chain.

At the basis of safe food production practises is the design and manufacture of products with a good safety record. When new products are developed, informed and qualified judgement which considers potential microbiological hazards and the necessary control measures as part of the HACCP concept is used. The hazard analysis part is often referred to as a safety assessment (refers to assessments of product safety by qualified persons on the basis of HACCP and knowledge/experience).

Generally, food industry conducts a safety assessment when designing new products, utilizing new production processes or changing manufacturing specifications. Use is made of scientific knowledge as well as of practical experience, for instance with particular raw material suppliers, the hygienic layout of the premises and the hygienic design of the equipment of the manufacturer. In many cases, safety assessments are supported by collective experience provided by organizations such as trade associations, food research institutes, governmental/regulatory bodies, academia, etc.). Safety assessments may combine qualitative and quantitative elements.

Traditionally the food industry is involved in the exposure assessment phase of risk assessment, and they have been driving developments in that area for many decades. On the other hand, governmental bodies and the academic community have made significant advances in the risk characterization phase. As the food industry is not involved or qualified in all phases of risk assessment, it is not evident that the industry can or should adopt the full risk assessment approach as the method by which the safety of food products is assessed.

Certainly in the manufacturing phase, HACCP is recognized by the food industry as the global standard for safeguarding food safety. Changes in the manufacturing specifications are dealt with through re-evaluation of HACCP plans, following a safety assessment approach. HACCP is very specific for the food product and processing site, an essential feature of its value and success. It should be stressed that hazard analysis is not a qualitative but a quantitative exercise. As expressed by the ICMSF as early as 1988, "the analysis of hazards must be quantitative if it is to be meaningful". This point is raised here because there is a persistent misconception that HACCP is qualitative and that risk assessment is quantitative. Likewise, the concept of an "acceptable level of a hazard" is as fundamental to the HACCP concept as "acceptable level of risk" is to the risk assessment concept. However, with the latter, it should be realized that the two concepts are different and need to be kept as separate systems because they serve different purposes. Through HACCP, industrial safety assessment assures the production of safe food products focussing on a single product and production site. MRA, as described by Codex, takes a broader view and considers safe food production in the larger context encompassing groups of similar food products, multiple producers and/or specific consumer populations.

The differences between a governmental risk assessment and the use of MRA by industry are outlined in Table 1. There are certain elements and aspects of MRA as used by governments that the food industry could benefit from, particularly in the pre-market phase where the safety of the design of a new product and/or manufacturing process needs to be assured. These include the following:

The extent to which industry can benefit from elements of MRA will depend on an industry’s or producer’s capabilities and capacities to identify the relevant benefits. Small businesses in many cases will not be able to benefit unless supporting organizations help and facilitate. Many small businesses or even larger companies are only beginning to use tools such as predictive models and thus the use of the new MRA tools will not happen in the immediate future.

Table 1. Differences between governmental (quantitative) Microbiological Risk Assessments and the use of elements of MRA in the food industry.

Governmental MRA

Industry using MRA elements

Purpose:

· Consumer health and safety protection & common concept for world trade issues

· Basis for Risk Management decision on Appropriate Level of Protection and Food Safety Objective

· Means to re-evaluate current food safety practices on the market

Purpose:

· Aid to built in safety and to engineer out hazards in new food products before marketing by using similar tools as used in MRA

· Transparency and auditability of the assessment study and the resulting HACCP plan

· Basis to re-evaluate food safety status of a product in future when necessary and for changing the HACCP plan accordingly

Scope:

· Consumer population nationally, regionally or globally

· Pathogen-pathway for a range of similar food products on a market made by different producers

· Risk Ranking, comparison risk of potential hazards in a foods/category or of a specific hazard in different foods/categories on the market

· Often a complete food chain (primary production to consumption) is covered

Scope:

· Consumer population in the intended market for a new product

· Pathogen-pathway for a specific product produced by of for a specific company

· Mostly covering hazard levels from raw material up to consumption

Input:

· Detailed data/knowledge on hazard dose-response effect in consumers, epidemiology and pathogenicity of hazard

· Typical or simulated data/knowledge on effect of producing, processing/product formulation/handling during and after manufacture

Input:

· No detailed data/knowledge on hazard dose-response effect in consumers, but generic epidemiology and pathogenicity of hazard, when available for the specific product - pathogen combination

· Typical/specific operational or simulated data/knowledge on raw material, effect of processing/product formulation and handling during and after manufacture, recontamination etc.

Output:

· A risk estimate in absolute or relative term

e.g. an estimation of the number of people in a population that may get a certain illness as the consequence of consuming a certain food containing a (certain level of a) certain pathogen

e.g. a categorization of different foods in order of increasing or decreasing relative risk

Output:

· The endpoint in general is the exposure assessment

· Food safety benchmarking is used to compare an estimated level of a certain pathogen in the food to be marketed with a similar food already on the market with a good safety record.


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