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Commission Regulation (EC) No 937/2001 of 11 May 2001 concerning the authorisation of new additive uses, new additive preparation, the prolongation of provisional authorisations and the 10 year authorisation of an additive in feedingstuffs (Text with EEA relevance) Official Journal L 130 , 12/05/2001 P. 0025 - 0032

Commission Regulation (EC) No 937/2001 of 11 May 2001 concerning the authorisation of new additive uses, new additive preparation, the prolongation of provisional authorisations and the 10 year authorisation of an additive in feedingstuffs (Text with EEA relevance) THE COMMISSION OF THE EUROPEAN COMMUNITIES, Having regard to the Treaty establishing the European Community, Having regard to Council Directive 70/524/EEC of 23 November 1970 concerning additives in feedingstuffs(1), as last amended by Commission Regulation (EC) No 2697/2000(2), and in particular Article 4 thereof, Whereas: (1) Directive 70/524/EEC provides that new additives and new uses of additives may be authorised following the review of an application made in accordance with Article 4 of the Directive. (2) Article 9e(1) of the Directive provides that provisional authorisation of a new additive or new use of an additive may be given if the conditions of Article 3a(b) to (e) are satisfied and if it is reasonable to assume, in view of the available results, that when used in animal nutrition it has one of the effects referred to in Article 2(a). Such provisional authorisation may be given for a period up to four years in the case of additives referred to in Part II of Annex C to the Directive. (3) The assessment of the dossiers submitted in respect of the new uses of the enzyme and micro-organism preparations described in Annexes I and II shows that they satisfy the abovementioned conditions and may therefore be authorised on a provisional basis for a four-year period. (4) New data were submitted to extend the authorisation of an enzyme preparation provisionally listed under No 11 to a new physical form. The assessment of the dossier submitted shows that the new physical form may be provisionally authorised. (5) On 1 October 2000, the authorisation of the micro-organism preparation No 1 Bacillus cereus var. toyoi (NCIMB 40 112) was provisionally renewed for a limited period, in order to provide sufficient time for the safety reassessment of the strain with regard to production of toxins, as requested in the opinion of the Scientific Committee for Animal Nutrition (SCAN) on the safety of use of bacillus species in animal nutrition adopted on 17 February 2000. (6) According to the SCAN opinion on Bacillus cereus var. toyoi (NCIMB 40 112) adopted on 21 March 2001, the assessment of the dossiers submitted shows that the product may be considered safe as regard toxin production. The provisional authorisation of the product may therefore be resumed. (7) Article 2(aaa) of Directive 70/524/EEC requires authorisations for coccidiostats to be linked to the person responsible for putting them into circulation. (8) Article 9b of Directive 70/524/EEC provides that the authorisations of such substances shall be given for a period of 10 years from the date on which final authorisation takes effect, if all conditions laid down in Article 3a of Directive 70/524/EEC are met. (9) The assessment of the dossier submitted shows that the coccidiostat described in Annex IV satisfies all the requirements of Article 3a, when used in the animal category and under the conditions described in the said Annex. (10) The assessment of the dossier shows that certain procedures may be required to protect workers from exposure to the additives. Such protection should however be assured by the application of Council Directive 89/391/EEC of 12 June 1989 on the introduction of measures to encourage improvements in the safety and health of workers at work(3). (11) The Scientific Committee for Animal Nutrition has delivered a favourable opinion with regard to the safety of the enzyme and micro-organism preparations and of the coccidiostat, and with regard to the favourable effect on animal production of the latter, under the conditions described in the said Annex. (12) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee for Feedingstuffs, HAS ADOPTED THIS REGULATION: Article 1 The preparations belonging to the group "Enzymes" listed in Annex I to the present Regulation are authorised for use as additives in animal nutrition under the conditions laid down in the Annex. Article 2 The preparations belonging to the group "Micro-organism" listed in Annex II to the present Regulation are authorised for use as additives in animal nutrition under the conditions laid down in the Annex. Article 3 The provisional authorisations of the preparation belonging to the group "Micro-organisms" listed in Annex III are resumed under the conditions laid down in the Annex. Article 4 The additive belonging to the "Coccidiostats and other medicinal substances" listed in Annex IV to the present Regulation is authorised for use as additive in animal nutrition under the conditions laid down in that Annex. Article 5 This Regulation shall enter into force on the day following that of its publication in the Official Journal of the European Communities. It shall apply from 1 June 2001. This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 11 May 2001. For the Commission David Byrne Member of the Commission (1) OJ L 270, 14.12.1970, p. 1. (2) OJ L 319, 16.12.2000, p. 1. (3) OJ L 183, 29.6.1989, p. 1. ANNEX I >TABLE> ANNEX II >TABLE> ANNEX III >TABLE> ANNEX IV >TABLE>

Commission Regulation (EC) No 937/2001

of 11 May 2001

concerning the authorisation of new additive uses, new additive preparation, the prolongation of provisional authorisations and the 10 year authorisation of an additive in feedingstuffs

(Text with EEA relevance)

THE COMMISSION OF THE EUROPEAN COMMUNITIES,

Having regard to the Treaty establishing the European Community,

Having regard to Council Directive 70/524/EEC of 23 November 1970 concerning additives in feedingstuffs(1), as last amended by Commission Regulation (EC) No 2697/2000(2), and in particular Article 4 thereof,

Whereas:

(1) Directive 70/524/EEC provides that new additives and new uses of additives may be authorised following the review of an application made in accordance with Article 4 of the Directive.

(2) Article 9e(1) of the Directive provides that provisional authorisation of a new additive or new use of an additive may be given if the conditions of Article 3a(b) to (e) are satisfied and if it is reasonable to assume, in view of the available results, that when used in animal nutrition it has one of the effects referred to in Article 2(a). Such provisional authorisation may be given for a period up to four years in the case of additives referred to in Part II of Annex C to the Directive.

(3) The assessment of the dossiers submitted in respect of the new uses of the enzyme and micro-organism preparations described in Annexes I and II shows that they satisfy the abovementioned conditions and may therefore be authorised on a provisional basis for a four-year period.

(4) New data were submitted to extend the authorisation of an enzyme preparation provisionally listed under No 11 to a new physical form. The assessment of the dossier submitted shows that the new physical form may be provisionally authorised.

(5) On 1 October 2000, the authorisation of the micro-organism preparation No 1 Bacillus cereus var. toyoi (NCIMB 40 112) was provisionally renewed for a limited period, in order to provide sufficient time for the safety reassessment of the strain with regard to production of toxins, as requested in the opinion of the Scientific Committee for Animal Nutrition (SCAN) on the safety of use of bacillus species in animal nutrition adopted on 17 February 2000.

(6) According to the SCAN opinion on Bacillus cereus var. toyoi (NCIMB 40 112) adopted on 21 March 2001, the assessment of the dossiers submitted shows that the product may be considered safe as regard toxin production. The provisional authorisation of the product may therefore be resumed.

(7) Article 2(aaa) of Directive 70/524/EEC requires authorisations for coccidiostats to be linked to the person responsible for putting them into circulation.

(8) Article 9b of Directive 70/524/EEC provides that the authorisations of such substances shall be given for a period of 10 years from the date on which final authorisation takes effect, if all conditions laid down in Article 3a of Directive 70/524/EEC are met.

(9) The assessment of the dossier submitted shows that the coccidiostat described in Annex IV satisfies all the requirements of Article 3a, when used in the animal category and under the conditions described in the said Annex.

(10) The assessment of the dossier shows that certain procedures may be required to protect workers from exposure to the additives. Such protection should however be assured by the application of Council Directive 89/391/EEC of 12 June 1989 on the introduction of measures to encourage improvements in the safety and health of workers at work(3).

(11) The Scientific Committee for Animal Nutrition has delivered a favourable opinion with regard to the safety of the enzyme and micro-organism preparations and of the coccidiostat, and with regard to the favourable effect on animal production of the latter, under the conditions described in the said Annex.

(12) The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee for Feedingstuffs,

HAS ADOPTED THIS REGULATION:

Article 1

The preparations belonging to the group "Enzymes" listed in Annex I to the present Regulation are authorised for use as additives in animal nutrition under the conditions laid down in the Annex.

Article 2

The preparations belonging to the group "Micro-organism" listed in Annex II to the present Regulation are authorised for use as additives in animal nutrition under the conditions laid down in the Annex.

The provisional authorisations of the preparation belonging to the group "Micro-organisms" listed in Annex III are resumed under the conditions laid down in the Annex.

Article 4

The additive belonging to the "Coccidiostats and other medicinal substances" listed in Annex IV to the present Regulation is authorised for use as additive in animal nutrition under the conditions laid down in that Annex.

Article 5

This Regulation shall enter into force on the day following that of its publication in the Official Journal of the European Communities.

It shall apply from 1 June 2001.

This Regulation shall be binding in its entirety and directly applicable in all Member States.

Done at Brussels, 11 May 2001.

For the Commission

David Byrne

Member of the Commission

(1) OJ L 270, 14.12.1970, p. 1.

(2) OJ L 319, 16.12.2000, p. 1.

(3) OJ L 183, 29.6.1989, p. 1.

ANNEX I

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ANNEX II

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ANNEX III

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ANNEX IV

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