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
28 - 30 April 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
Related events
Towards a Biobased Chemical Future
26 February 2026 13:00-17:00, London, United Kingdom
Carbon Capture or Carbon Fiction? Science, Policy, and the UK’s Methane Blind Spot
26 March 2026 17:45-20:45, London, United Kingdom
The 59th Annual International Meeting of the ESR Spectroscopy Group of the 91AV
13 April 2026 15:00 - 16 April 2026 23:00, Colchester, United Kingdom
What a chemist needs to know about Patents 2026
13 May 2026 09:00-17:40, London, United Kingdom
Search
Advertisement
Spotlight
Explore
Membership
