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  • 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.