SCHEDULE 5AMENDMENTS
24.
(a)
“(b)
a person specially authorised by the product licence or by the marketing authorisation to which the Marketing Authorisations for Veterinary Medicinal Products Regulations 1994 apply in respect of that drug to sell the drug under the alternative product name specified in the licence or marketing authorisation;”;
(b)
in article 2(1) in the definition of “veterinary drug” after the words “in respect of which a product licence” there shall be inserted the words “or a marketing authorisation”;
(c)
in article 3 after the words “holder of the product licence”, in each place where they occur, there shall be inserted the words “or marketing authorisation”;
(d)
in article 6(1) after the words “holder of a product licence” there shall be inserted the words “or marketing authorisation”;
(e)
in article 9 after the words “product licence”, in each place where they occur, there shall be inserted the words “or marketing authorisation”;
(f)
in article 11(1) after the words “product licence” there shall be inserted the words “or marketing authorisation”; and
(g)
in Schedules 1, 2, 3 and 4 for the words “product licence no.”, in each place where they occur, there shall be substituted the words “product licence/marketing authorisation no.”.