SCHEDULES
SCHEDULE 7Qualified persons
PART 3Obligations of qualified person
13.
(1)
This paragraph applies where—
(a)
a medicinal product which has undergone the controls referred to in paragraph 12 in another member State is imported to the United Kingdom; and
(b)
each batch of the product is accompanied by control reports signed by another qualified person in respect of the medicinal product.
(2)
Where this paragraph applies, the qualified person is not responsible for carrying out the controls referred to in paragraph 12.