This module reviews the principal qualitative and quantitative analytical methods in common use, the principles of method selection and validation. It also includes, sampling plans, physical and organoleptic testing, stability testing and the significance of degradation, contamination and adulteration of pharmaceutical materials. Importantly, it also includes the interpretation of analytical data including non conforming results and stresses the importance of how these need to be managed.
QP Analysis and Testing - includes practical day
20 - 22 October 2014, Reading, United Kingdom
Introduction
Venue
The Science & Technology Centre
The Science & Technology Centre, Earley Gate, Whiteknights Road, Reading, RG6 6BZ, United Kingdom
Organised by
Reading Scientific Services Ltd
Contact information
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