Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

Please note this session will be run online over Microsoft Teams - further details will be sent directly to attendees.


  • Understanding the documentation required in relation to IMP for requesting trial authorisation
  • Understanding the need for a manufacturing licence for IMPs
  • Understanding the difference between QP Declaration certificates and QP Release certificates
  • The need for Certificate of Analysis documentation
  • Drug accountability logs
  • Special licence for the use of Specials
  • The difference between an IMP and a NIMP

Places must be booked for this course. 

Please email to reserve your space. A University/NHS email address should be used when making your booking.