SCHEDULE 6Exemptions for small pet animals
ManufactureE13
F11
The product must have been manufactured by—
a
the holder of a manufacturing authorisation if manufactured in F4Great Britain;
F3b
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F5c
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
d
in the case of any other country, a manufacturer whose premises have been inspected and approved by an officer of the Secretary of State.
F62
Sub-paragraph (1)(d) does not apply where the United Kingdom has a formal agreement with the exporting country that includes mutual recognition of good manufacturing practice or where the Secretary of State is satisfied that the exporting country requires manufacturers of veterinary medicinal products to apply standards of good manufacturing practice which are at least equivalent to those in Great Britain.
ManufactureE23
The product must have been manufactured by—
a
the holder of a manufacturing authorisation if manufactured in the United Kingdom;
b
the holder of a manufacturing authorisation issued under Directive 2001/82/EC if manufactured in F2a member State;
c
in the case of Australia, Canada, New Zealand, or Switzerland, the holder of an authorisation from the competent authority permitting the manufacture of medicinal products;
d
in the case of any other country, a manufacturer whose premises have been inspected and approved by an officer of the Secretary of State.