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Pharmaceutical Stability Testing

9 Module eBook

Online Learning

Take this 9-module ebook and learn how to conduct timely, effective and compliant stability studies to enhance your pharmaceutical development programme.

Work through the course at your own pace online, test your knowledge with end of module quizzes and receive a certificate once you've passed the final course quizzes. This course is available for individual registrations or can be supplied to a department as a licence for a year.

For more information about our eBook capabilities click on the key features.

  • Develop the optimal stability programme design for early stage development
  • Gain clarification of the ICH Q1A regulatory guidelines to ensure complete compliance
  • Learn practical tips for conducting effective photostability studies
  • Achieve successful reporting of stability data within ICH Q1E guidelines
  • Reduce the analytical burden by implementing bracketing and matrixing design approaches
  • Design meaningful and compliant forced degradation studies
  • Practical tips for maintaining stability chambers and studies over long periods of time

This course is highly recommended for anyone working in pharmaceuticals, in the following departments, fields or positions:

  • Stability
  • Analytical Chemistry/Methods
  • Formulation Development
  • QA/QC
  • Manufacturing/Production
  • Method Validation
  • Regulatory Affairs
  • GMP Compliance
  • Chemical Engineering
  • Development/Chemistry
  • Outsourcing
  • R&D Analyst / Assistant
  • Stability Officer / Supervisor / Analyst/ Coordinator
  • Analytical Development Engineer

Dr. Geoff Carr

Dr Geoff Carr was appointed as Manager, Analytical Development at Patheon Inc, Ontario, Canada in 2000 and is now Director, Analytical Development.


Prior to that, he held positions of Manager, Analytical Sciences at Celltech-Chiroscience, UK, Head of Analytical Development at Medgenix, Belgium and before that at Wyeth Research, UK. He originally started his career in pharmaceutical analysis at The British Pharmacopoeia Laboratory where he held several posts and was finally appointed Head of the Laboratory.
He has been a Member of various British Pharmacopoeia Committees and a UK representative to Committees of the European Pharmacopoeia and is now a Member of the General Chapters Expert Committee of USP.

 

Lorraine Jackson

Lorraine Jackson is a regulatory consultant with 6 years’ experience and a strong scientific background. Lorraine  joined Gregory Fryer Associates, Cambridge, UK in 2008 and now holds the position of Senior Regulatory Consultant and Team Leader.


Prior to this, Lorraine worked for 12 years in a successful bio-pharmaceutical company, UCB-Celltech, having held the position of  Senior group leader in Analytical, Quality and Regulatory Operations.  Lorraine is a registered member of TOPRA, The Organisation for Professionals in Regulatory Affairs  and has extensive expertise in preparation of regulatory submissions throughout Europe and the US.

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