SCHEDULE 2The manufacture of veterinary medicinal products
PART 3Authorisation of blood banks
Labelling
22.
(1)
The operator of a blood bank must ensure that every container used for the blood is labelled with—
(a)
the identification of the donor animal;
(b)
the date of collection;
(c)
the authorisation number of the blood bank;
(d)
any necessary warnings;
(e)
the expiry date.
(2)
There must be no specific therapeutic indication on the label or on any information relating to the product.
(3)
It is an offence to fail to comply with this paragraph.