The QP should be aware of the different requirements between commercial and clinical trial
operations. This one day course examines EU legislation and GMP issues, many of which are
unique and associated with Investigational Medicinal Products (IMPs). It will provide practical
guidance on the major differences between IMPs and commercial operations. Delegates will
also have the opportunity to learn about the principles of Good Clinical and Good Laboratory
Practice. The course is ideally suited for those wishing to ensure they have sufficient awareness
of the specific nature of IMPs and the challenges facing the QP.
operations. This one day course examines EU legislation and GMP issues, many of which are
unique and associated with Investigational Medicinal Products (IMPs). It will provide practical
guidance on the major differences between IMPs and commercial operations. Delegates will
also have the opportunity to learn about the principles of Good Clinical and Good Laboratory
Practice. The course is ideally suited for those wishing to ensure they have sufficient awareness
of the specific nature of IMPs and the challenges facing the QP.
