Commission Regulation (EU) No 142/2011Dangos y teitl llawn

Commission Regulation (EU) No 142/2011 of 25 February 2011 implementing Regulation (EC) No 1069/2009 of the European Parliament and of the Council laying down health rules as regards animal by-products and derived products not intended for human consumption and implementing Council Directive 97/78/EC as regards certain samples and items exempt from veterinary checks at the border under that Directive (Text with EEA relevance)

Article 27U.K.Importation [F1from a third country] and transit of research and diagnostic samples

1.The competent authority may authorise the importation [F2from a third country] and the transit of research and diagnostic samples, comprising derived products or animal by-products, including the animal by-products referred to in Article 25(1), in accordance with conditions which ensure the control of risks to public and animal health.

Such conditions shall include at least the following:

(a)the introduction of the consignment must have been authorised in advance by the competent authority of the [F3constituent nation] of destination; and

(b)the consignment must be sent directly from the point of entry into [F4Great Britain] to the authorised user.

F52.. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

3.Operators handling research samples or diagnostic samples [F6from a third country] shall comply with the special requirements for disposal of research and diagnostic samples set out in Section 1 of Chapter III of Annex XIV hereto.

Textual Amendments