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PART 2U.K.Authorised veterinary medicinal products

Placing a veterinary medicinal product on the marketE+W+S

4.[F1(1) No person may place a veterinary medicinal product on the market unless the Secretary of State has—

(a)as regards a product to which Schedule 1B applies, issued a QNIG certificate in respect of that product;

(b)otherwise, granted a marketing authorisation in respect of that product.]

(2) No person may certify data in relation to an application for a marketing authorisation or in relation to an existing marketing authorisation if they know that those data are false, or do not believe that they are accurate.

(3) Schedule 1 (marketing authorisations) has effect.

[F2(4) Schedule 1A (converted EU marketing authorisations) has effect.]

[F3(5) Schedule 1B (Northern Ireland qualifying good marketing authorisations) has effect. ]

Placing a veterinary medicinal product on the marketN.I.

4.—(1) No person may place a veterinary medicinal product on the market unless that product has been granted a marketing authorisation by the Secretary of State or the Agency.

(2) No person may certify data in relation to an application for a marketing authorisation or in relation to an existing marketing authorisation if they know that those data are false, or do not believe that they are accurate.

(3) Schedule 1 (marketing authorisations) has effect.

Extent Information

E2This version of this provision extends to Northern Ireland only; a separate version has been created for England and Wales and Scotland only