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Introduction

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.

Useful links

Downloads

• RSSL Training QP12.pdf

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

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