The Methodology for Calculating Stability and Release limits
Estimating Shelf Life and Post-licensure Stability Studies
Investigation of OOS and OOT Stability Results
Outsourcing Stability Studies - Achieving Successful Relationships and Outcomes
Implementation of a Flexible cGMP Complaint Stability Program for Phase I - III Studies
Stability Chambers
Temperature Monitoring During Transportation and Storage
Assessing the Stability of Amorphous or Semi-Amorphous Materials
Integrating Laboratory Information Management Systems to Optimize Stability Programs
Forced Degradation Studies of API s and Drug Products
Stress Testing of APIs and Drug Products
Overcoming Key Challenges in Stability Testing for Generics
Current Practices in Annual Vaccine Stability Studies
Past Events
Biopharmaceutical & Pharmaceutical Stability Current Trends & Best Practices - 23-24 Mar 2010, Jersey City, New Jersey, United States (2343)
Important
Please, check "Biopharmaceutical & Pharmaceutical Stability Current Trends & Best Practices" official website for possible changes, before making any traveling arrangements
