12. In regulation 21 (records by a holder of a manufacturing authorisation)—
(a)for paragraph (1) substitute—
“(1) The holder of a manufacturing authorisation must record the following information in respect of any veterinary medicinal product supplied by the holder—
(a)the name of the veterinary medicinal product and marketing authorisation number if applicable;
(b)the pharmaceutical form and strength of the product;
(c)the quantity of product supplied;
(d)the batch number and expiry date;
(e)the date of the transaction under which the product was supplied;
(f)the company name and the permanent address or registered place of business of the recipient of the supply.”;
(b)in paragraph (3) at the end insert “or for one year after the date of expiry of the batch, whichever is the longer.”.