4.—(1) The manufacturing authorisation shall specify—
(a)the types of veterinary medicinal products and pharmaceutical forms that may be manufactured or imported;
(b)the place where they are to be manufactured or controlled;
(c)the name and address of the person holding the authorisation;
(d)the address of the premises to which it relates;
(e)the name of the qualified person nominated to act under this Schedule.
(2) It may specify that different activities must be carried out in different premises or parts of premises, and may require the holder of the manufacturing authorisation to restrict access to premises or parts of premises to persons carrying out activities there.