The QP needs to have an understanding of the different requirements between commercial and clinical trial operations. This module examines the EU legislation relevant to Investigational Medicinal Products (IMPs), their manufacture, control and supply. Practical guidance on the major differences in GMP expectations between IMPs and commercial products will be given.
QP Course - Investigational Medicinal Products (Additional Knowledge)
4 December 2012, Reading, United Kingdom
Introduction
Venue
RSSL Pharma Training
RSSL Pharma Training, Whiteknights Road, Reading, RG6 6BZ, United Kingdom
Useful links
Organised by
RSSL Pharma Training
Contact information
Mrs Rachel Horton
Reading Scientific Services Ltd, The Reading Science Centre, Whiteknights Campus, Reading, RG6 6LA, United Kingdom
0118 9184024
Contact us by email
Reading Scientific Services Ltd, The Reading Science Centre, Whiteknights Campus, Reading, RG6 6LA, United Kingdom
0118 9184024
Contact us by email
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