
Article 1 
Regulation (EC) No 853/2004 is amended as follows:

1.. Annex II is amended in accordance with Annex I to this Regulation.
2.. Annex III is amended in accordance with Annex II to this Regulation.
Article 2 
This Regulation shall enter into force on the seventh day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.Done at Brussels, 6 November 2006.
For the Commission
Markos KYPRIANOU
Member of the Commission
ANNEX I

Section I, Part A, point (2) of Annex II to Regulation (EC) No 853/2004 is replaced by the following:
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2. However, when a product's packaging and/or wrapping is removed or it is further processed in another establishment, a new mark must be applied to the product. In such cases, the new mark must indicate the approval number of the establishment where these operations take place.
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ANNEX II

Annex III to Regulation (EC) No 853/2004 is amended as follows:

1.. In Section I, Chapter IV is amended as follows:

((a)) Point 8 is replaced by the following:
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8. Carcases and other parts of the body intended for human consumption must be completely skinned, except in the case of porcine animals, the heads of ovine and caprine animals and calves, the muzzle and lips of bovine animals and the feet of bovine, ovine and caprine animals. Heads, including muzzle and lips, and feet must be handled in such a way as to avoid contamination.
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((b)) Point 16(a) is replaced by the following:
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((a)) the tonsils of bovine animals, porcine animals and solipeds must be removed hygienically;'.
2.. In Section VIII, Chapter III, Part E is added as follows:
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E. 
Food business operators must ensure that raw materials used in the preparation of fish oil for human consumption comply with the following requirements:


1.. they must derive from fishery products which have been found fit for human consumption;
2.. they must come from establishments, including vessels, approved in accordance with this Regulation;
3.. they must be transported and stored until processing in hygienic conditions.
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3.. Section IX is replaced by the following:
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SECTION IX: RAW MILK, COLOSTRUM, DAIRY PRODUCTS AND COLOSTRUM-BASED PRODUCTS For the purpose of this Section,

1.. “Colostrum” means the fluid secreted by the mammary glands of milk-producing animals up to three to five days post parturition that is rich in antibodies and minerals, and precedes the production of raw milk.
2.. “Colostrum-based products” means processed products resulting from the processing of colostrum or from the further processing of such processed products.
 CHAPTER I: RAW MILK AND COLOSTRUM — PRIMARY PRODUCTION Food business operators producing or, as appropriate, collecting raw milk and colostrum must ensure compliance with the requirements laid down in this Chapter.
 I.  1. 

((a)) that do not show any symptoms of infectious diseases communicable to humans through milk and colostrum;
((b)) that are in a good general state of health, present no sign of disease that might result in the contamination of milk and colostrum and, in particular, are not suffering from any infection of the genital tract with discharge, enteritis with diarrhoea and fever, or a recognisable inflammation of the udder;
((c)) that do not have any udder wound likely to affect the milk and colostrum;
((d)) to which no unauthorised substances or products have been administered and that have not undergone illegal treatment within the meaning of Directive 96/23/EC;
((e)) in respect of which, where authorised products or substances have been administered, the withdrawal periods prescribed for these products or substances have been observed.
 2. 
((a)) In particular, as regards brucellosis, raw milk and colostrum must come from:

((i)) cows or buffaloes belonging to a herd which, within the meaning of Directive 64/432/EEC, is free or officially free of brucellosis;
((ii)) sheep or goats belonging to a holding officially free or free of brucellosis within the meaning of Directive 91/68/EEC; or
((iii)) females of other species belonging, for species susceptible to brucellosis, to herds regularly checked for that disease under a control plan that the competent authority has approved.
((b)) As regards tuberculosis, raw milk and colostrum must come from:

((i)) cows or buffaloes belonging to a herd which, within the meaning of Directive 64/432/EEC, is officially free of tuberculosis; or
((ii)) females of other species belonging, for species susceptible to tuberculosis, to herds regularly checked for this disease under a control plan that the competent authority has approved.
((c)) If goats are kept together with cows, such goats must be inspected and tested for tuberculosis.
 3. 

((a)) in the case of cows or buffaloes that do not show a positive reaction to tests for tuberculosis or brucellosis, nor any symptoms of these diseases, after having undergone a heat treatment such as to show a negative reaction to the alkaline phosphatase test;
((b)) in the case of sheep or goats that do not show a positive reaction to tests for brucellosis, or which have been vaccinated against brucellosis as part of an approved eradication programme, and which do not show any symptom of that disease, either:

((i)) for the manufacture of cheese with a maturation period of at least two months; or
((ii)) after having undergone heat treatment such as to show a negative reaction to the alkaline phosphatase test; and
((c)) in the case of females of other species that do not show a positive reaction to tests for tuberculosis or brucellosis, nor any symptoms of these diseases, but belong to a herd where brucellosis or tuberculosis has been detected after the checks referred to in point 2(a)(iii) or 2(b)(ii), if treated to ensure its safety.
 4. Raw milk and colostrum from any animal not complying with the appropriate requirements of points 1 to 3, and in particular, any animal showing individually a positive reaction to the prophylactic tests vis-à-vis tuberculosis or brucellosis as laid down in Directive 64/432/EEC and Directive 91/68/EEC, must not be used for human consumption.
 5. The isolation of animals that are infected, or suspected of being infected, with any of the diseases referred to in point 1 or 2 must be effective to avoid any adverse effect on other animals' milk and colostrum.
 II.  A.  1. Milking equipment and premises where milk and colostrum are stored, handled or cooled must be located and constructed so as to limit the risk of contamination of milk and colostrum.
 2. Premises for the storage of milk and colostrum must be protected against vermin, have adequate separation from premises where animals are housed and, where necessary to meet the requirements laid down in Part B, have suitable refrigeration equipment.
 3. Surfaces of equipment that are intended to come into contact with milk and colostrum (utensils, containers, tanks, etc. intended for milking, collection or transport) must be easy to clean and, where necessary, disinfect and must be maintained in a sound condition. This requires the use of smooth, washable and non-toxic materials.
 4. After use, such surfaces must be cleaned and, where necessary, disinfected. After each journey, or after each series of journeys when the period of time between unloading and the following loading is very short, but in all cases at least once a day, containers and tanks used for the transport of milk and colostrum must be cleaned and disinfected in an appropriate manner before re-use.
 B.  1. 

((a)) that, before milking starts, the teats, udder and adjacent parts are clean;
((b)) that milk and colostrum from each animal is checked for organoleptic or physico-chemical abnormalities by the milker or a method achieving similar results and that milk and colostrum presenting such abnormalities is not used for human consumption;
((c)) that milk and colostrum from animals showing clinical signs of udder disease are not used for human consumption otherwise than in accordance with the instructions of a veterinarian;
((d)) the identification of animals undergoing medical treatment likely to transfer residues to the milk and colostrum, and that milk and colostrum obtained from such animals before the end of the prescribed withdrawal period are not used for human consumption; and
((e)) that teat dips or sprays are used only after authorisation or registration in accordance with the procedures laid down in Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market:
((f)) that colostrum is milked separately and not mixed together with raw milk.
 2. 

((a)) Milk must be cooled immediately to not more than 8 oC in the case of daily collection, or not more than 6 oC if collection is not daily;
((b)) Colostrum must be stored separately and immediately cooled to not more than 8 oC in the case of daily collection, or not more than 6 oC if collection is not daily, or frozen.
 3. During transport the cold chain must be maintained and, on arrival at the establishment of destination, the temperature of the milk and the colostrum must not be more than 10 oC.
 4. 

((a)) the milk is processed within two hours of milking; or
((b)) a higher temperature is necessary for technological reasons related to the manufacture of certain dairy products and the competent authority so authorises.
 C.  1. Persons performing milking and/or handling raw milk and colostrum must wear suitable clean clothes.
 2. Persons performing milking must maintain a high degree of personal cleanliness. Suitable facilities must be available near the place of milking to enable persons performing milking and handling raw milk and colostrum to wash their hands and arms.
 III.  1. 
((a)) The following criteria for raw milk apply pending the establishment of standards in the context of more specific legislation on the quality of milk and dairy products.
((b)) National criteria for colostrum, as regards plate count, somatic cell count or antibiotic residues, apply pending the establishment of specific Community legislation.
 2. 

((a)) the food business operator producing the milk;
((b)) the food business operator collecting or processing the milk;
((c)) a group of food business operators; or
((d)) in the context of a national or regional control scheme.
 3. 
((a)) Food business operators must initiate procedures to ensure that raw milk meets the following criteria:

((i)) for raw cows' milk:

Plate count at 30 oC (per ml) ≤ 100 000
Somatic cell count (per ml) ≤ 400 000


((ii)) for raw milk from other species:

Plate count at 30 oC (per ml) ≤ 1 500 000

((b)) However, if raw milk from species other than cows is intended for the manufacture of products made with raw milk by a process that does not involve any heat treatment, food business operators must take steps to ensure that the raw milk used meets the following criterion:

Plate count at 30 oC (per ml) ≤ 500 000

 4. 

((a)) it contains antibiotic residues in a quantity that, in respect of any one of the substances referred to in Annexes I and III to Regulation (EEC) No 2377/90, exceeds the levels authorised under that Regulation; or
((b)) the combined total of residues of antibiotic substances exceeds any maximum permitted value.
 5. When raw milk fails to comply with point 3 or 4, the food business operator must inform the competent authority and take measures to correct the situation.
 CHAPTER II: REQUIREMENTS CONCERNING DAIRY AND COLOSTRUM-BASED PRODUCTS  I.  1. 

((a)) milk is quickly cooled to not more than 6 oC;
((b)) colostrum is quickly cooled to not more than 6 oC or maintained frozen,

and kept at that temperature until processed.
 2. 

((a)) processing begins immediately after milking, or within four hours of acceptance at the processing establishment; or
((b)) the competent authority authorises a higher temperature for technological reasons concerning the manufacture of certain dairy or colostrum-based products.
 II.  1. 

((a)) Pasteurisation is achieved by a treatment involving:

((i)) a high temperature for a short time (at least 72 oC for 15 seconds);
((ii)) a low temperature for a long time (at least 63 oC for 30 minutes); or
((iii)) any other combination of time-temperature conditions to obtain an equivalent effect,

such that the products show, where applicable, a negative reaction to an alkaline phosphatase test immediately after such treatment.


((b)) Ultra high temperature (UHT) treatment is achieved by a treatment:

((i)) involving a continuous flow of heat at a high temperature for a short time (not less than 135 oC in combination with a suitable holding time) such that there are no viable microorganisms or spores capable of growing in the treated product when kept in an aseptic closed container at ambient temperature, and
((ii)) sufficient to ensure that the products remain microbiologically stable after incubating for 15 days at 30 oC in closed containers or for seven days at 55 oC in closed containers or after any other method demonstrating that the appropriate heat treatment has been applied.
 2. 

((a)) have regard to the procedures developed in accordance with the HACCP principles pursuant to Regulation (EC) No 852/2004; and
((b)) comply with any requirements that the competent authority may impose in this regard when approving establishments or carrying out checks in accordance with Regulation (EC) No 854/2004.
 III.  1. 

((a)) raw cows' milk used to prepare dairy products has a plate count at 30 oC of less than 300 000 per ml; and
((b)) processed cows' milk used to prepare dairy products has a plate count at 30 oC of less than 100 000 per ml.
 2. When milk fails to meet the criteria laid down in paragraph 1, the food business operator must inform the competent authority and take measures to correct the situation.
 CHAPTER III: WRAPPING AND PACKAGING Sealing of consumer packages must be carried out immediately after filling in the establishment where the last heat treatment of liquid dairy products and colostrum-based products, takes place by means of sealing devices that prevent contamination. The sealing system must be designed in such a way that, after opening, the evidence of its opening remains clear and easy to check.
 CHAPTER IV: LABELLING  1. 

((a)) in the case of raw milk intended for direct human consumption, the words “raw milk”;
((b)) in the case of products made with raw milk, the manufacturing process for which does not include any heat treatment or any physical or chemical treatment, the words “made with raw milk”;
((c)) in case of colostrum, the word “colostrum”;
((d)) in case of products made with colostrum, the words “made with colostrum”.
 2. The requirements of paragraph 1 apply to products destined for retail trade. The term “labelling” includes any packaging, document, notice, label, ring or collar accompanying or referring to such products.
 CHAPTER V: IDENTIFICATION MARKING By way of derogation from the requirements of Annex II, Section I:

1.. rather than indicating the approval number of the establishment, the identification mark may include a reference to where on the wrapping or packaging the approval number of the establishment is indicated;
2.. in the case of the reusable bottles, the identification mark may indicate only the initials of the consigning country and the approval number of the establishment.
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4.. In Section XV, Chapter III, point 1 is replaced by the following:
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1. Collagen must be produced by a process that ensures that the raw material is subjected to a treatment involving washing, pH adjustment using acid or alkali followed by one or more rinses, filtration and extrusion or by an approved equivalent process. The extrusion step may be not carried out when manufacturing low molecular collagen from raw materials of non-ruminant origin.
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