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Stability Testing in Pharmaceutical Development and Manufacturing

5 - 6 June 2014, Amsterdam, Netherlands


Introduction
This course has been updated to reflect the recent changes in the pharmaceutical stability testing world.
The new course content will provide a comprehensive update on current trends which offer substantial potential savings in time and resources in a traditionally costly testing area. It will include opportunities for review of specific participant problems

The course will cover:
* Recent regulatory changes affecting stability including
* The implications of implementation of ICH Q7, Q8, Q9, Q10 and Q11 for stability testing
* Changes to European GMP guidance with impact on stability testing including Annexe updates affecting product development, outsourcing and application of Quality Risk Management (QRM)
* Product Quality Reviews and the interpretation of stability data.

Recent scientific developments with implications for stability, with a particular focus on cost reduction, shortening of development timelines, and improvements on existing interpretation systems
* ASAP - using short term high stress testing to get accurate predictions of shelf life with a high degree of confidence – Freethink Technologies' ASAPprime®
* Low level impurities and their impact on product stability
* Manipulation of tablet internal pH to improve product stability

Useful links

Venue
Hotel Amsterdam

Hotel Amsterdam, 93-94 Damrak, Amsterdam, 1012 LP, Netherlands

Organised by
PharmaTraining
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