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Regulation (EC) No 1774/2002 of the European Parliament and of the Council of 3 October 2002 laying down health rules concerning animal by-products not intended for human consumption (repealed)
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Version Superseded: 15/03/2005
Point in time view as at 01/01/2005.
There are currently no known outstanding effects for the Regulation (EC) No 1774/2002 of the European Parliament and of the Council (repealed), ANNEX V.
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[F1premises for the processing of animal by-products must not be at the same site as slaughterhouses, unless located in a completely separate building. However, a conveyer system may link an individual processing plant to a slaughterhouse on the same site provided the following conditions are met:
there are separate entrances, reception bays, equipment, exits and personnel for the processing plant and the slaughterhouse; and
the animal by-products to be processed originate on the same premises.
Unauthorised persons and animals must not have access to the processing plant;]
the processing plant must have a clean and unclean sector, adequately separated. The unclean sector must have a covered place to receive animal by-products and must be constructed in such a way that it is easy to clean and disinfect. Floors must be laid in such a way as to facilitate the draining of liquids. The processing plant must have adequate lavatories, changing rooms and washbasins for staff;
the processing plant must have sufficient production capacity for hot water and steam for the processing of animal by-products;
the unclean sector must, if appropriate, contain equipment to reduce the size of animal by-products and equipment for loading the crushed animal by-products into the processing unit;
all installations in which animal by-products are processed must operate in accordance with the requirements of Chapter II. Where heat treatment is required, all installations must be equipped with:
measuring equipment to monitor temperature against time and, if necessary, pressure at critical points;
recording devices to record continuously the results of these measurements; and
an adequate safety system to prevent insufficient heating;
to prevent recontamination of the finished product by incoming animal by-products, there must be a clear separation between the area of the plant where incoming material for processing is unloaded and the areas set aside for the processing of that product and the storage of the processed product.
Textual Amendments
50 mm in case of heat treatment in accordance with paragraph 2(a); or
30 mm in case of heat treatment in accordance with paragraph 2(b).
They must then be mixed with formic acid to reduce and maintain the pH to 4,0 or lower. The mixture must be stored for at least 24 hours pending further treatment.
a core temperature of at least 90 °C for at least 60 minutes; or
a core temperature of at least 70 °C for at least 60 minutes.
When using a continuous flow system, the progression of the product through the heat converter must be controlled by means of mechanical commands limiting its displacement in such a way that at the end of the heat treatment operation the product has undergone a cycle which is sufficient in both time and temperature.]
Textual Amendments
F2 Substituted by Commission Regulation (EC) No 93/2005 of 19 January 2005 amending Regulation (EC) No 1774/2002 of the European Parliament and of the Council as regards processing of animal by-products of fish origin and commercial documents for the transportation of animal by-products (Text with EEA relevance).
Samples of material taken directly after heat treatment:
Clostridium perfringens absent in 1 g of the products
Samples of material taken during or upon withdrawal from storage at the processing plant:
Salmonella: absence in 25 g: n = 5, c = 0, m = 0, M = 0
Enterobacteriaceae: n = 5, c = 2, m = 10, M = 300 in 1 g
where:
=
number of samples to be tested;
=
threshold value for the number of bacteria; the result is considered satisfactory if the number of bacteria in all samples does not exceed m;
=
maximum value for the number of bacteria; the result is considered unsatisfactory if the number of bacteria in one or more samples is M or more; and
=
number of samples the bacterial count of which may be between m and M, the sample still being considered acceptable if the bacterial count of the other samples is m or less.
check:
the general conditions of hygiene of the premises, equipment and staff;
the efficacy of the own checks carried out by the plant, in accordance with Article 25, particularly by examining the results and taking samples;
the standards of the products after processing. The analyses and tests must be carried out in accordance with scientifically-recognised methods (in particular, those laid down in Community legislation or, where none exist, recognised international standards or, in their absence, national standards); and
the storage conditions;
take any samples required for laboratory tests; and
make any other checks it considers necessary to ensure compliance with this Regulation.
description of the process (by a process flow diagram);
identification of critical control points (CCPs) including the material process rate for continuous systems;
compliance with the specific process requirements laid down by this Regulation; and
achievement of the following requirements:
particle size for batch-pressure and continuous processes — defined by the mincer hole or the anvil gap size, and
temperature, pressure, processing time and material processing rate (for continuous system only) as specified in paragraphs 2 and 3.
the temperature must be monitored with a permanent thermocouple and it must be plotted against real time;
the pressure stage must be monitored with a permanent pressure gauge. Pressure must be plotted against real time;
the processing time must be shown by time/temperature and time/pressure diagrams.
At least once a year the thermocouple and the pressure gauge must be calibrated.
the temperature and the pressure must be monitored with thermocouples, or an infrared temperature gun, and pressure gauges used at defined positions throughout the process system in such a way that temperature and pressure comply with the required conditions inside the whole continuous system or in a section of it. The temperature and pressure must be plotted against real time;
measurement of the minimum transit time inside the whole relevant part of the continuous system where the temperature and pressure comply with the required conditions, must be provided to the competent authorities, using insoluble markers (for example, manganese dioxide) or a method which offers equivalent guarantees. Accurate measurement and control of the material process rate is essential and must be measured during the validation test in relation to a CCP that can be continuously monitored such as:
feed screw revolutions per minute (rev./min.),
electric power (amps at given voltage),
evaporation/condensation rate, or
number of pump strokes per unit time.
All measuring and monitoring equipment must be calibrated at least once a year.
‘Saturated steam’ means that all air is evacuated and replaced by steam in the whole sterilisation chamber.
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