The Veterinary Medicines Regulations 2013 No. 2033

SCHEDULE 2 The manufacture of veterinary medicinal products

PART 5 Authorisation of equine stem cell centres

Labelling

32.—(1) The operator of an equine stem cell centre must ensure that every container used for the stem cell product is labelled with—

(a) the identification of the donor animal;

(b) the date of collection;

(c) the authorisation number of the equine stem cell centre;

(d) any necessary warnings;

(e) the expiry date.

(2) The operator of an equine stem cell centre must ensure that no specific therapeutic indication is included on the label or on any information relating to the product.