The Medicines for Human Use (Clinical Trials) Regulations 2004 No. 1031

SCHEDULE 7 STANDARD PROVISIONS FOR MANUFACTURING AUTHORISATIONS

PART 3 PROVISIONS WHICH MAY BE INCORPORATED IN AN AUTHORISATION RELATING TO THE IMPORTATION OF INVESTIGATIONAL MEDICINAL PRODUCTS

3.  The holder of the authorisation shall provide such information as may be requested by the licensing authority concerning the type and quantity of any investigational medicinal products which he imports.