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  1. Hace 2 días · It also verified the reports on the method of analysis of the feed additive in feed submitted by the Reference Laboratory set up by Regulation (EC) No 1831/2003. The assessment of L-valine produced by Corynebacterium glutamicum CGMCC 7.358 shows that the conditions for authorisation, as provided for in Article 5 of Regulation (EC) No 1831/2003, are satisfied.

  2. Hace 5 días · Regulation (EC) No 1831/2003 - On additives for use in animal nutrition. Regulation (EC) No 178/2002 - Laying down the general principals and requirements of food law, establishing the...

  3. Hace 5 días · According to Article 8 of Regulation (EC) No 1831/2003, EFSA, after verifying the particulars and documents submitted by the applicant, shall undertake an assessment in order to determine whether the feed additive complies with the conditions laid down in Article 5.

  4. Hace 1 día · TechnoSpore® (Bacillus coagulans DSM 32016), submitted for authorization by Biochem Zusatzstoffe Handels- und Produktionsges. mbH is evaluated under the European Commission’s Regulation (EC) No 1831/2003 for use as a zootechnical feed additive in piglets, growing Suidae, chickens for fattening, other poultry, and ornamental birds.

  5. opmaat.sdu.nl › content › CELEX-32024R1201-20240519-ENGSdu

    Hace 3 días · Regulation (EC) No 1831/2003 provides for the authorisation of additives for use in animal nutrition and for the grounds and procedures for granting such authorisation. In particular, Article 10(2) of that Regulation provides rules for the re-evaluation of additives authorised pursuant to Council Directive 70/524/EEC (2) .

  6. Hace 2 días · MSs should ensure that the procedure for granting a MA is completed within a maximum of 210 days after the submission of a valid application. Clock stops are possible. Legal basis: Artl. 8, 17, Directive 2001/83/EC; for variations: Artl. 4 (1), 5 (1) and 6 (1) of Regulation (EC) No 1084/2003. 1.4.

  7. Hace 2 días · The single public interface for all information related to EFSA’s scientific work. Follow the risk assessment process from receipt of the dossier to adoption of the opinion: status of assessments, dossier and studies (non-confidential versions), meetings agenda and minutes, info on experts, etc...