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