The Quality Control Laboratory, in both the R & D and Operations environment, is a key element of the supply chain and has a particularly significant impact on lead times, affecting speed of drug development and overall site manufacturing performance. As the UK pharmaceutical industry faces ever-increasing competition from abroad, the enhancement of laboratory productivity to improve the product-process development cycle and manufacturing efficiency has become even more crucial for the long-term viability of UK-based sites.This symposium will review advances in laboratory efficiency which, both individually and collectively, are designed to achieve these outcomes, through the adoption of process-based improvement tools, automation and integrated data handling within the laboratory.
Advances in pharmaceutical laboratory efficiency
16 October 2008, London, United Kingdom
Introduction
Venue
Royal Pharmaceutical Society of Great Britain
Royal Pharmaceutical Society of Great Britain, 1 Lambeth High Street, London, SE1 7JN, United Kingdom
Organised by
The Joint Pharmaceutical Analysis Group
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