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Stability Testing in Pharmaceutical Development and Manufacturing

17 October 2019 09:00 - 18 October 2019 17:00, London, United Kingdom


Introduction
The course will cover:
The impact of the lifecycle approach on product development:
  • 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, statistics, 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 - 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
 
Speakers
  • Dr Michael Gamlen United Kingdom

Venue
HILTON LONDON EUSTON Hotel

HILTON LONDON EUSTON Hotel, 17-18 Woburn Place, London, WC1H 0HT, United Kingdom

Useful links

Organised by
PharmaCourses Ltd
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