Join Dr. Mark Powell as he looks at the various stability studies conducted from the start of pharmaceutical development to the manufacture of marketed product. Dr. Mark Powell will also explain the purpose of each study and highlight some of the potential pitfalls.
Topics covered include:
• Aims of stability evaluation
• The effect of environmental factors and the primary pack
• API stability
• Excipient compatibility
• Prototype stability (including accelerated stability using the ASAP model and stress stability studies)
• Bulk hold studies
• In-use stability
• Registration stability
• Shipping excursion studies.
This webinar is hosted by Q1 Scientific, a global leader in environmentally controlled stability storage and sample management.