SCHEDULE 2The manufacture of veterinary medicinal products
F1PART 2AActive Substances
F1Prohibition on manufacture, importation or distribution of active substances unless registeredE126
1
No person may manufacture, import or distribute an active substance unless the person is registered in the register maintained under sub-paragraph (2).
2
The Secretary of State must establish and maintain a register of manufacturers, importers and distributors of active substances and the sites occupied by them for the purposes of manufacturing or holding active substances.
LabellingE226
The authorised person must ensure that, before a veterinary medicinal product is supplied, every container is labelled with—
a
the name of the veterinary surgeon who ordered the veterinary medicinal product;
b
a precise description of the veterinary medicinal product;
c
the date of production;
d
the name of the authorisation holder and the address of the authorised premises;
e
the expiry date;
f
any necessary warnings; and
g
instructions for use.
Sch. 2 Pts. 2A (paras. 26-31), 2B (para. 32) inserted (E.W.S.) (17.5.2024) by The Veterinary Medicines (Amendment etc.) Regulations 2024 (S.I. 2024/567), regs. 1(1), 93