SCHEDULE 1STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE RELATING TO THE MANUFACTURE AND ASSEMBLY OF RELEVANT MEDICINAL PRODUCTS

4.  The manufacturer’s licence holder shall inform the licensing authority of any change that he proposes to make to any personnel named in his licence as respectively—

(a)responsible for supervising the production operations;

(b)in charge of the animals from which are derived any substances used in the production of the medicinal products being manufactured or assembled; or

(c)responsible for the culture of any living tissues used in the manufacture of the medicinal products being manufactured or assembled.